Cytokinetics is a biopharmaceutical company founded in 1997. Specializing in muscle biology and the potential treatment of serious diseases, Cytokinetics aims to develop innovative therapies that could transform the lives of patients. With a focus on muscle function and the biology of muscle contraction, the company is dedicated to advancing the field of muscle biology research and drug development.

Associate Director, Packaging and Serialization

Senior Director, US Field Excellence & Operations

Associate Director, Clinical Data Management - External Data Solutions

Associate Director, Commercial Learning & Development

Senior Director, Business Insights and Analytics

Director Regulatory Writing (Medical Writer)

Director, Aficamten Global Marketing and Commercial Strategy

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM), Bayern, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Bayern

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM), Saarland, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Saarland

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. The Director, HR Business Partner DACH serves as the strategic HR partner for Germany, Austria, and Switzerland, supporting the company’s first EU commercial launch planned for 2026–2027. Reporting to the Head of HR, Europe with dotted line to VP, GM DACH, this role is responsible for shaping and executing the full end-to-end HR agenda for the region, ensuring organizational readiness, leadership capability, and cultural alignment as the business scales. This position operates within a newly evolving European HR operating model and works in close partnership with business leaders, the European HR team, and global HR Centers of Excellence (CoEs) to deliver consistent, high-impact people solutions while addressing local market needs. Responsibilities Serve as the primary HR partner and steward of the full HR agenda for the DACH region, ensuring alignment with European and global business objectives. Partner with senior business leaders to drive performance, organizational capability, and commercial launch readiness, providing strategic counsel through periods of growth and change. Act as a trusted advisor to leaders, influencing decision-making and reinforcing the desired leadership culture and ways of working. Co-own and drive talent, organizational effectiveness, and culture-building initiatives aligned with European and global HR strategy. Lead workforce planning, organizational design, role creation, and headcount planning to support near- and long-term business growth. Support succession planning, leadership development, and long-term talent strategies to ensure leadership continuity and bench strength. Own staffing plans and recruiting pipeline quality for the DACH region, partnering closely with Talent Acquisition and HR Centers of Excellence to deliver high-quality hiring outcomes. Participate in hiring decisions for critical and leadership roles, ensuring alignment with capability, culture, and future-state organizational needs. Lead annual performance management processes, including goal setting, performance reviews, calibration, and development planning. Manage salary and bonus cycles in alignment with regional reward frameworks and corporate guidelines. Coach managers on performance planning, career development, and effective leadership behaviors, building leadership capability across the organization. Ensure consistent deployment of HR systems, policies, reward programs, and people processes in alignment with European and corporate standards, while addressing local requirements. Implement and sustain HR initiatives delivered by HR Centers of Excellence, ensuring effective adoption and change management at the local level. Contribute to European and global HR projects and cross-functional initiatives, representing DACH business needs and perspectives. Develop and execute the annual HR Business Plan aligned with European HR priorities and business objectives. Provide support for HR administration management as required, ensuring compliance, efficiency, and a positive employee experience. Qualifications 10+ years of progressive HR Business Partner or HR Generalist experience with increasing scope, complexity, and leadership responsibility. Bachelor’s degree in Human Resources, Business Administration, or a related field; advanced degree (Master’s or MBA) preferred. Biopharmaceutical or pharmaceutical industry experience strongly preferred, ideally within a commercial environment. Proven success as a strategic HR partner in a build-out, scale-up, or first-market commercial launch environment. Demonstrated experience partnering effectively with HR Centers of Excellence in a global, matrixed organization. Deep knowledge of German labor law, co-determination principles, and works council engagement; experience supporting German-based employee populations required. Strong consulting, communication, and influencing skills, with the ability to operate credibly with senior leaders and cross-functional stakeholders. Experience operating across multiple countries and cultures, with sensitivity to regional and local market dynamics. Strong business acumen with the ability to translate business strategy into people and organizational solutions. Demonstrated change leadership capability, including experience leading organizations through growth, transformation, or ambiguity. Experience leveraging HR systems and tools, such as HRIS (e.g., Workday or equivalent), performance management and talent platforms, compensation planning tools, and workforce analytics, to inform decision-making, ensure compliance, and drive scalable people processes. Fluency in German and English strongly preferred. #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Director, Human Resources Business Partner, DACH

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. The Medical Scientist will work as a member of the Medical team to support Cytokinetics portfolio with products in different phases of lifecycle and relay field-based clinical/medical insights back to Cytokinetics to impact the future strategy so Cytokinetics can continue to bring innovative medicines to patients with cardiac diseases. Reporting to the Associate Medical Director and in close cross-functional alignment, the Medical Scientist is a scientific professional who serves as a key field-based scientific resource for healthcare providers, patients, industry partners and internal colleagues. This role will come with high visibility in our company with critical cross-functional relationships across Medical Affairs, Clinical Development / Operations, and Commercial.&nbsp; This role will focus on key opinion leaders and other HCPs in the cardiovascular space and especially in the hypertrophic cardiomyopathy therapeutic area, but also support pipeline products in development. Our passion is anchored in rigorous and diligent scientific and clinical approaches to the discovery and development of novel mechanism therapeutics. With gratitude for the commitments and convictions of our employees who are inspired by the courage of patients we aim to serve, we believe Cytokinetics will continue to be a pioneering, values-driven, sustainable, fully integrated biopharmaceutical company. &nbsp; Role and Responsibilities Identify national, regional, and local Key Opinion Leaders (KOLs) involved in Expert Centers of cardiomyopathy and engage them in proactive and reactive scientific exchange Maintain and enhance existing scientific collaboration and professional relationships with hospital-based HCPs in priority but also office-based HCPs within a defined geography (physicians, genetic counselors, nurses, payers, pharmacists, hospital teams, investigators, etc..) involved in the therapeutic management of patients with cardiac diseases to expand research, advisory, and educational partnership opportunities; identify areas of unmet medical need; and assure thoughtful exchange of current medical information related to products in development and therapeutic areas of importance Facilitate access to educational grant request process and facilitate alignment of IIP (Investigator-initiated Program) activities with internal areas of scientific interest. Serve as the primary Cytokinetics external Medical Affairs representative for key stakeholders in assigned territories, providing deep and advanced disease state and product information as well as facilitating collaborations aligning with Cytokinetics’ strategic goals. Ensure prompt intake and responses for medical information and requests for Medical Affairs support. Serve as a scientific expert within the country and Europe (when needed) at key medical and scientific conferences, advisory boards, clinical investigator meetings, internal meetings, and patient advocacy group meetings Consistently collect, report and represent clinical insights and unanswered questions received from external contacts to the appropriate channels internally. Conduct routine literature searches and communicate regularly with each other to assure that the entire Medical team benefits from individual learning whenever it is relevant. Build and maintain a high-level of scientific knowledge and understanding about disease state, underlying science, treatment guidelines, available treatment agents and options, as well as heart failure and hypertrophic cardiomyopathy therapies under development. Maintain a superior understanding of current trends in clinical research, competitive developments, patient care, and their impact on Cytokinetics’ medical strategies Work with Medical Affairs and other internal colleagues on initiatives including medical information, publications, medical education, grants, speaker training, and other educational programs both within the country and internationally Provide initial and ongoing disease and product training to internal and field personnel. Provide support to our clinical development programs by serving as a key point of contact for company-sponsored trial investigators, investigator-initiated research, and registries consistent with company objectives and regulations Generate Field Medical Affairs plans to identify collaborative opportunities with KOL’s and institutions Identify congresses and scientific national and international meetings that are interesting and relevant to attend. Review scientific program of relevant conferences, attend sessions, support exhibit booth operations, and contribute to a timely written conference report summarizing key information, activities, and competitive intelligence to colleagues Document accurately and timely his/her activities within applicable company databases and platforms The Medical Scientist role entails not only scientific and customer expertise, &nbsp;but also requires the ability to understand and effectively utilize approved resources to fulfill administrative, procedural, and legal requirements in order to address the customer needs. These activities may include proficiency in computer skills and database entry, continual compliance of all procedural requirements of the role and appropriate utilization of available resources. Ensure compliance with all Cytokinetics policies and procedures as well as local regulatory and legal requirements. Educational requirements&nbsp; Advanced biomedical sciences degree (Dipl., MD, PharmD, PhD, Bachelor's + Master's degree in science (5 years of higher education) Professional work experience&nbsp; Medical Affairs experience (minimum 3 years), with field experience, within biotechnology or pharmaceutical industry and a record of significant accomplishment: Experienced MSL, Medical Advisor, Medical Manager or similar with thorough understanding of the biopharmaceutical industry Experience in cardiac diseases (hypertrophic cardiomyopathy/heart failure) and/or rare diseases is preferred In depth knowledge of Medical Affairs organizations, including related operating processes, policies, procedures and regulations Knowledge of applicable pharmaceutical regulations as well as other industry rules and guidelines along with medical and clinical terminology knowledge Strong business acumen; has working knowledge of the multi-disciplinary functions involved in a company's drug development process, e.g. research, development, clinical operations, biostatistics, regulatory, commercial Personal attributes Must be analytical and articulate in both oral and written communications, possess excellent presentation and listening skills, with a demonstrated ability to communicate well with external stakeholders and all internal levels of the organization Native country language speaker and high proficiency in English language Proven planning and organizational skills Proven ability to collaborate and make connections with both internal and external stakeholders Stellar interpersonal skills, customer focus and emotional intelligence in developing and maintaining professional relationships Thrives in a team environment Proven self-starter that is solution focused when presented with challenges Ability to manage a demanding schedule, and adapt and be flexible as needed with evolving priorities Proficiency with Microsoft Office and web-based applications A valid driver’s License is required Ability to travel both domestically (up to 80%) and internationally on occasion #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Medical Science Liaison (TMS)

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. Reporting to the Senior Medical Director France Benelux, the Associate Medical Director France role will not only be customer facing with medical field team responsibility for roll out but also strategic, to support implementation and execution of the devised medical launch strategy for CYTK products in France.&nbsp; The Associate Medical Director will serve as national lead of a team consisting of scientific professionals who serve as a key field-based scientific resource for healthcare providers, patients, industry partners and internal colleagues. In this role, the individual will lead field medical operations and manage a field-based French Medical Science Liaison (MSL) team. The Associate Medical Director will collaborate and actively support the cross-functional team with the execution of the medical strategy in France and provide input relevant to France and Europe, based on their local expertise and insights. The Associate Medical Director will be a key role in the ongoing build out of the wider planned French medical affairs team. Responsibilities Subject matter expert in HCM disease state and its management in France as well as on aficamten and its competitors In collaboration with the French Benelux Sr. MD, strategize on the development of the country medical affairs plan and implementation of a field Medical Affairs vision and strategy, in alignment with the company’s corporate strategies and objectives. Lead field medical operations as the company’s field-based Medical Affairs team leader, participating directly in KOL/HCP development and engagement as well as supporting ongoing early and late-stage clinical trials in his region. Lead field medical launch-related planning for aficamten (a cardiac myosin inhibitor) being developed for obstructive hypertrophic cardiomyopathy (oHCM). Ensure the MSL team is continuously trained on emerging aficamten data as it’s presented at congresses &amp; via scientific publications and incorporate such data into the MSL aficamten Communication Plan. Foster a compliant, cross-functional, customer-centric team approach between the TMS team and other Cytokinetics field-based teams/roles as the company transitions from Research &amp; Development to a Commercial organization. Manage and mentor a MSL team while providing strong leadership to develop and motivate the MSL team to meet and exceed key performance indicators (KPIs). Clearly communicate national and local TMS goals, objectives, and KPIs. Actively support the TMS team and their efforts by advocating and promoting collaboration within the team, across internal working groups, and with customers. Guide and assist the TMS team in key opinion leader and expert cardiologist engagement in the field and with internal stakeholders. Establish and maintain collaborative relationships with targeted scientific leaders to develop potential scientific and clinical therapeutic ideas related to hypertrophic cardiomyopathy (HCM) and heart failure (HF)), including coordination/support of investigator-initiated, non-registration pre-clinical and/or clinical studies. In close collaboration with international and global team establish a CRM system in France and being the responsible person for this in France Ensure that all MSL interactions and activities adhere to corporate and healthcare compliance guidance, including those related to scientific interactions with internal and external groups, responses to unsolicited requests for medical/scientific information, and discussion of external research. Collect insights from the field and sensitize the MSLs on competitive intelligence Facilitate a training strategy for disease state and portfolio/pipeline products to enhance MSL team knowledge. Maintain clinical, scientific, and technical expertise in cardiovascular medicine. Serve as a scientific resource to internal functional areas within Cytokinetics including serving as a member of cross-functional teams as required. Work with Medical Affairs and other internal, cross-functional colleagues on initiatives including congress planning, medical information, publications, medical education, and speaker training, as well as align priorities around areas of research interest. Train and organize the MSL team to effectively support congress activities like booth duty, scientific session coverage, KOL engagement, competitive intelligence collection, etc. Support planning, execution and leadership French advisory boards to gather feedback and input on study design, clinical trial data, clinical experience and medical education. Provide medical input and support to the commercial and market access activities for France Ability to travel regularly as required, region wide and globally, as necessary for business needs and development support Collaborate and work closely with all necessary related and associated departments including Marketing, Regulatory, Legal, Market Access and Pharmacovigilance Ensure that any associated needs of health care professionals and other key customers in France are known, understood and addressed in right time and in a compliant manner Qualifications Advanced Medical or scientific degree (MD, PhD, PharmD) 10+ Years working at Medical Affairs Manager/Ass. Director level within pharma/biotech Demonstrated leadership skills, with a successful track record in managing/coordinating field-based medical teams or medical science liaisons (MSL). Experience in Cardiology or related specialities and/or in rare cardiovascular diseases is advantageous Launch experience/expertise, ideally in specialty care is highly advantageous Strong understanding of the healthcare landscape, regulatory environment, and medical practices within France Excellent communication and presentation skills in both French and English, with the ability to effectively convey complex scientific information to diverse audiences. Proven expertise in KOL engagement, medical strategy, and collaboration with cross-functional teams. Proven ability to build strong relationships with KOLs and HCPs&nbsp; Ability to manage multiple priorities and manage time efficiently &nbsp;High ethical standards and familiarity with compliance guidelines in medical affairs Ability to work on their own, take initiative and accountability Strong ability to work remotely and adapt to a changing environment Ability to travel mostly national and if required in EU or globally Experience with Veeva or another CRM system #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Associate Medical Director

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Cytokinetics (Italy) S.rl. is seeking an experienced and energetic Administrative / Office Assistant&nbsp; to join their newly created and growing Italian team. Reporting directly to the General Manager Italy, the candidate will support the team by managing relevant business administrative processes, critical internal and external meetings and events, and will be the key contact for the Milan based office, in combination with options to work remotely. Operating within a regulated pharmaceutical environment, the role supports governance, compliance, and business continuity through professional coordination of executive activities, facilities management, and stakeholder engagement. ROLE RESPONSIBILITIES Manage critical business administrative processes, including: Vendor, contract, purchase order (PO), and invoice management in internal systems, in collaboration with the Finance team. &nbsp; Manage invoice tracking versus budgets, and accruals. Contract management with external parties in close collaboration with the Legal &nbsp; department, including an audit-proof filing system. Plan and organize team meetings and internal events, including venue selection, agency/vendor contracting, and ensuring fun and engaging team-building elements. Ensure follow-up on action items post-meeting. Basic project management for external events (e.g. booking meetings, venues, logistics and vendor management) involving healthcare professionals (HCPs), such as congresses, symposia, educational events and expert meetings, in close collaboration with Commercial and Medical Affairs teams. Assist People Managers with onboarding new team members by organizing workplaces and IT equipment. Introducing new colleagues to relevant business processes and systems Act as a point of contact for all Italian Cytokinetics Employees for all relevant HR stuff Interact with EU functions in Zug such as Finance, HR, Legal, Regulatory &amp; Compliance to ensure business continuity and compliance in Rules and Regulations. Coordinate roll-out, training and documentation of company SOPs. Perform general office duties such as answering phones, handling correspondence, and filing documents. Provide comprehensive PA and administrative support to the senior leaders based in Cytokinetics Italy office such as the General Manager, Medical Director and Commercial Director. Meeting coordination and project management support for the GM Italy. Be onsite at the Milan based Cytokinetics office 3 days a week as part of a functioning hybrid work environment for the team. &nbsp;REQUIRED QUALIFICATIONS Minimum of 4 years of experience in managing business processes in the healthcare and/or pharmaceutical industry sector. Proven track record of supporting senior management and broader teams in a hands-on, start-up-like environment. Solid knowledge and understanding of the Italian pharmaceutical compliance regulations. Exceptional multitasking and prioritization skills, with the ability to perform efficiently under pressure. Advanced proficiency with relevant office software applications and company administration/finance as well as contract management systems. Excellent interpersonal and organizational skills with self-confidence in building positive, productive working relationships across all levels. Outstanding written and oral communication skills in both Italian and English. Demonstrated project management experience, with strong planning and cross-functional coordination abilities. Highly structured, organized, efficient, solution-focused way of working and communicating. A self-starter with uncompromised personal integrity and reliability, who embodies the company’s ethical standards, professionalism, and core values. A committed ambassador of Cytokinetics core values.#LI-HYBRID Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Administrative / Office Assistant

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM), Hamburg, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Hamburg

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM), Sachsen, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Sachsen

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. Reporting directly to the Director of Global Logistics, the Senior Manager, Supply Chain Logistics is part of the wider Supply Chain team responsible for oversight of all movements Globally related to Cytokinetics commercial products. Additionally, the Senior Manager, Supply Chain Logistics, will support all other non-commercial movements and ensure all movements are undertaken in accordance with the appropriate approved vendors &amp; shipping conditions specific to the product or material and in compliance with Good Distribution Practice (GDP). The key responsibilities assigned to the Senior Manager, Supply Chain Logistics can be divided into areas of focus as follows: Transportation and Shipping Storage and Distribution Trade Compliance Responsibilities Ensure all commercial material movements are undertaken in accordance with the appropriate storage &amp; shipping conditions specific to the product or material and in compliance with Good Distribution Practice (GDP). Support R&amp;D teams for Sample and non-commercial movements in accordance with the appropriate storage &amp; shipping conditions specific to the product or material and in compliance with Good Distribution Practice (GDP). Support logistics activities across the entire supply chain for all products up to the stage that products reach the Cytokinetics 3PL’s. Oversight of and support of ongoing Global Shipping Validation Maintenance activities. Liaison with Quality department for all logistics related activities such as SOP, Change Control, Deviation, CAPA. Support the monthly inventory reconciliation process in cooperation with the finance team. Ensure appropriate Trade compliance documentation, international trade and customs requirements, are in place to support all product shipments. Ensure all US material imports comply with the Automated Commercial Environment (ACE) requirements of the FDA &amp; CBP. Manage Distribution Operations as required to meet the growth of business in EU, UK, Switzerland Markets. Execute distribution strategy with 3PL and Wholesalers, to ensure support and availability of all products. Work cross-functionally with Supply Chain on CMO projects, product shipment logistics, inventory levels, and inventory tracking. Work closely with Supply Chain, Quality and Finance to ensure the successful distribution of all Cytokinetics products to direct purchasing customers. Work closely with the Commercial Sales leadership to maintain customer satisfaction. Adhere to relevant regulatory and compliance guidelines and Company policies. Qualifications Bachelor's degree in supply chain management, operations management, engineering, business 5 years industry experience of logistics and distribution of products in a commercial pharmaceutical environment. Experience in virtual manufacturing, e.g. managing outsourced business services including 3rd party manufacturing, supplier, transportation, warehousing &amp; distribution. Strong understanding of pharmaceutical regulations, Good Distribution Practice (GDP), Good Manufacturing Practice (GMP), and other relevant industry standards. Strong problem-solving abilities, attention to detail, and ability to make data-driven decisions. Excellent verbal and written communication skills, with the ability to interact with internal teams, external partners, and regulatory bodies. Strong organizational skills with the ability to manage multiple projects and deadlines effectively. Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Senior Manager, Supply Chain Logistic

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. As the Associate Director, External Manufacturing and Supply Operations, you are responsible for operational execution of external manufacturing and related supply activities. This is a central role within Manufacturing and External Supply Operations and requires the ability to manage multiple activities simultaneously, balancing priorities, with a strong sense of urgency, ability to work with ambiguity, and attention to detail. This position will have you collaborating with other members of Supply Chain, Quality Assurance, Regulatory Affairs, and Finance to execute and deliver endorsed global supply plans for both clinical and commercial supply. You will report to the Director, External Supply Operations. Responsibilities Build and maintain productive relationships with external contract manufacturers (CMO’s), and internal global colleagues Ensure timely and effective execution of all manufacturing and supply plans at assigned CMO’s Develop and manage production processes to support operational execution, including BOM’s, specifications, CAPA’s, change controls, master data, and artwork. Familiarity with ERP/MRP systems Support logistics, transportation and import/export activities Act as the manufacturing and supply chain representative for review and approval of documentation including but not limited to batch records, BOM’s, specifications, artwork, and change control Support product qualification activities including but not limited to reviewing/approving IQ/OQ/PQs, stability, and validation protocols; review and approve change controls Play a key role in supporting selection and onboarding of new CMOs, technical transfers, operationalizing product supply and site establishment Manage and track inventory, perform inventory reconciliations, and support month end close process. Issue purchase orders, and track invoices and budgets Maintain production schedules and track batch record execution in coordination with Quality Oversee, review, and approve as necessary revisions to manufacturing cGMP and non GMP documentation Proven risk management acumen with a continuous improvement mindset Where necessary, provide input to the manufacturer and QA for evaluation of process deviations and assist in the investigation of product complaints Build and maintain strong partnerships and provide effective communication with all internal and external stakeholders and lead discussion, problem solving efforts and process improvements to ensure that performance targets are met or exceeded Responsible for scheduling and maintaining routine business operations meetings with CMO’s Support Regulatory submissions and CMC as required Qualifications BS/BA Degree in Life Science, Biology, or Engineering discipline from an accredited college or university, or equivalent desired 10+ years combined experience in manufacturing, outsourced operations, technical operations and/or supply chain in regulated healthcare industry, preferably within biotech/pharmaceutical industry cGMP career experience embedded in a pharmaceutical manufacturing plant is essential – with first-hand knowledge of plant operations, with the insight to assess performance, and diagnose issues directly at the source Technical background with knowledge of engineering and pharmaceutical manufacturing processes in small molecule is required, and experience in DS/API production is desirable Excellent problem-solving skills, with the ability to address complex challenges under time pressure Demonstrated expertise in risk management, with a history of successfully implementing risk mitigation strategies The ability to function in a fast-paced, high-growth, entrepreneurial environment Ability to travel domestically and internationally ~25% Position requires a strong working knowledge and understanding of both regional and international regulations by government agencies affecting the pharmaceutical industry (CFR's, EU GMP, ICH) Timely and effective communication across multiple audiences, both verbally and in writing &nbsp; &nbsp;Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Associate Director, External Manufacturing and Supply Operations

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Reporting directly to the VP, General Manager, DACH, with a dotted line to the Head of Market Access Europe, and as a member of the DACH Leadership Team,&nbsp;the Director Market Access DACH will lead, plan and execute market access strategy, projects and initiatives in Germany, Austria and Switzerland, both on the national as well as on the regional, operative level. They will lead, coordinate and support the German Field Market Access team in their regional and local customer engagements, as well as collaboration with the commercial sales force. Ensuring alignment with the International Market Access team, the Market Access Director will be a dynamic and adaptable leader, responsible for implementing strategies and initiatives that enhance commercial success across all business areas in Germany, Austria and Switzerland. ROLE RESPONSIBILITIES Market Access and Reimbursement Strategy Support national reimbursement strategies across the DACH region, in close collaboration with the DACH leadership team, the company´s international market access functions, and the external market access consultants of the respective country. Support the development of value propositions, evidence packages and reimbursement submissions for favorable Health Technology Assessment (HTA) outcomes and pricing / reimbursement decisions with bodies such as IQWIG, Gemeinsamer Bundesausschuss (G-BA), GKV-SV (Spitzenverband der gesetzlichen Krankenkassen), on the AMNOG reimbursement process in Germany, as well as related institutions in Austria (Dachverband) and Switzerland (BAG). Pricing responsibilities will include pricing assumptions and scenarios for business review and development for the Regional &amp; Global Pricing Committee, when needed. Oversee and lead the planning and execution of pre-launch and launch market access activities. Drive successful launch readiness activities, including reimbursement and pricing negotiations with key regional stakeholders of the respective countries. Ensure pipeline products are appropriately included in country level horizon scanning processes. Develop and execute regional reimbursement strategies and innovative contracting approaches. Monitor and analyze national as well as regional healthcare developments, including cost-effectiveness, reimbursement pathways, early benefit assessments or changes in pharmaceutical funding or purchasing mechanisms. Report trends and adapt strategies, accordingly, in order to minimize price reductions or price reference range . Provide proactive insights and training to commercial team, on strategies to reduce prescription hurdles and enhance product uptake. Lead and Develop Teams The Director Market Access DACH will inspirationally lead the Field Market Access function in Germany, ensuring effective execution of regional access strategies across the 17 KV regions. This includes leading, instructing and training a team of Field Market Access Managers who engage with Commercial Key Account Managers, prescribers, regional payers, healthcare providers, and other key stakeholders to facilitate optimal reimbursement and access conditions for Cytokinetic´s products. The operative support of the Key Account Managers in the field via double visits of important prescribers will be particularly important to address any reimbursement concerns that limit the use of Cytokinetic´s products. Lead, coach, and develop a high-performing team of Field Market Access Managers across Germany. Provide ongoing training and development for the Field Market Access team and other customer-facing roles to ensure excellence in execution and stakeholder engagement. Stakeholder Engagement and Communication Establish and maintain trusted relationships with key opinion leaders (KOLs), sick funds, Regional Associations of SHI Physicians (KVen), regional payor bodies and other relevant stakeholders and decision makers across the DACH region. Understand and address stakeholder needs to support the adoption of innovative therapies. Represent the company in relevant industry associations, forums, and regional events of payers and policy makers. Ensure compliant engagement with external stakeholders, offering value-added services and addressing access barriers. Enhance the company’s reputation by positioning it as a trusted partner within the healthcare ecosystem in the DACH region. Cross-functional Collaboration Collaborate closely with national marketing, medical, sales teams, as well as international market access and HEOR functions, to ensure cohesive strategy execution. Support driving a Key Account Management strategy approach to the markets by integrating market access perspectives into cross-functional customer engagement plans. Facilitate communication and alignment between field and office-based teams. Manage local market access budgets and allocate resources effectively to meet strategic priorities. Data-Driven Decision Making Analyze and present data to inform strategic decisions and track performance against KPIs. Identify and communicate market access trends, opportunities, and risks to internal stakeholders. Communication and Enablement Create and deliver needs-oriented information materials that highlight the value of products and support effective communication with prescribers. Utilize both analog and digital channels to engage with networks and stakeholders effectively. QUALIFICATIONS AND EXPERIENCE Educational Background Bachelor's degree required; advanced university degree preferred, ideally in natural science, business administration, or healthcare-related field. Industry Experience 10+ years of experience in the pharmaceutical or biopharmaceutical industry within market access-related functions. Minimum of 3 years in regional market access or related roles, with demonstrated success in execution of market access strategies in the field on customer level. Healthcare System Expertise Deep understanding of the German, and basic understanding of the Austrian and Swiss healthcare systems, including legal frameworks for pricing and reimbursement. Strong network and stakeholder engagement experience with sick funds and other payor bodies in Germany. Operative experience in Austria and Switzerland is not a must, but beneficial. Stakeholder Management and Communication Proven experience in stakeholder management, with the ability to build resilient networks and influence decision-making. Strong communication and presentation skills, capable of translating complex topics into audience-appropriate formats. High motivation, goal orientation, and a team-oriented, independent working style. Cross-functional and Digital Competence Experience in matrixed, fast-paced organizations and managing cross-functional projects. IT-savvy, with proficiency in modern digital communication channels and MS Office applications. Language and Travel Native-level fluency in German and business-fluent English, both written and verbal. Willingness to travel regularly across the DACH region. What We Offer The privilege to participate in building and shaping the in-country operations of a young, dynamic company in the DACH region, assuming personal responsibility for business-critical projects and processes within a team of highly experienced professionals. An opportunity to join a scientifically outstanding, research-based specialty care pharmaceutical company, shaping the future of innovative treatments in muscle biology. A highly collaborative and inclusive environment which supports professional growth and personal development. A very competitive salary and benefits package above industry average. &nbsp; &nbsp;Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Director, Market Access DACH

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Reporting to the Executive Director, Regulatory Affairs - CMC, the Director of Regulatory Affairs-CMC is responsible for leading regulatory support for assigned programs to ensure sound regulatory planning and tactical implementation of US and international regulatory submission strategies. Responsibilities Formulate CMC regulatory strategies, without supervisor oversight, based on current regulatory intelligence. Collaborates with cross-functional project teams and external business partners to develop CMC regulatory strategies and identify regulatory risks; represents the department in cross-functional project teams. Identifies the required documentation and any content, quality and timeline issues for global submissions and manages the delivery of approved technical documents in accordance with project timelines. Manages the preparation, authoring and maintenance of regulatory submission documents pertaining to CMC data for global clinical trial and marketing applications, as well as post-marketing variations. May require technical regulatory authoring of submission package components. Supports the evaluation of manufacturing changes for the potential impact on products. Provides expert review of CMC documentation supporting regulatory submissions and communications. Coordinates preparation of responses to queries from regulatory authorities, particularly focused on CMC. May require technical regulatory authoring to support responses to queries. Maintains knowledge and expertise with FDA/EMA regulations, ICH guidelines and other international regulatory regulations and guidelines, as needed to support global programs. Ensures conformance to commitments made with various regulatory agencies (e.g., IND/CTA commitments) for assigned programs. Provides regulatory advice to other functional areas. May participate in regulatory due diligence activities. Relationships Build and maintain collaborative relationships with internal/external business partners to achieve project regulatory goals. Develops and maintains collaborative relationships with other departments to ensure effective communication regarding project regulatory goals, issues and timelines. Develop and manage relationships with external vendors and regulatory health authorities. Coordinates activities for meetings and conferences with FDA, EMA, and other regulatory authorities Collaborate with regulatory colleagues to provide CMC expertise as needed. Management This is an Individual Contributor position; however, there is the possibility for supervising consultants/contractors and/or interns. Develops and implements regulatory operating guidelines and common work practices/strategies within the team. Qualifications 10 - 12+ years of related work experience (Director candidates will typically bring 12+ years; Associate level candidates may be considered with 10+ years and strong potential), including 8+ years in Regulatory Affairs CMC in the Biotech/Pharmaceutical industry; experience in small molecule drug development required; experience in the cardiovascular therapeutic area is a plus Proven experience serving as a primary RA-CMC contact to Health Authorities, with full strategic responsibility. Bachelor’s degree is required, preferably in chemistry or a closely related field; advanced degree is a plus. Advanced degree is preferred. Excellent working knowledge of international regulatory requirements and environment, including an understanding of GXP Solid working knowledge of core processes associated with discovery, development, and manufacturing of small molecules. Experience with eCTD requirements and electronic submissions Experience with international regulatory submissions and processes is a strong plus. Ability to work effectively across teams, functions and with outside partners. Excellent oral and written communication skills Excellent organizational skills and attention to detail Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Director, Regulatory Affairs CMC

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. The Regional Sales Manager&nbsp;leads a high-performing team to drive growth across the region, with a strong focus on strategic execution, customer engagement, and cross-functional collaboration. This role is responsible for developing and executing business plans, cultivating relationships with key healthcare professionals, ensuring regulatory compliance, and fostering a results-oriented, patient-centric culture. This is a senior-level commercial leadership position within the pharmaceutical (biotech) industry, ideally suited for someone who thrives on high-level scientific exchange and finds purpose in bringing first-in-class treatments to patients—positively impacting their lives and those of their families. The Regional Sales Manager will lead a team of dedicated Key Account Managers within the assigned region. The role offers a high degree of autonomy and visibility, along with a unique opportunity to shape how Cytokinetics is positioned in the DACH region. ROLE RESPONSIBILITIES Leadership &amp; Team Development Recruit, lead, coach, and mentor a high-performing team of Key Account Managers. Conduct regular field visits and coaching sessions to ensure effective sales execution. Set and monitor individual and team goals, including incentive plans and development objectives. Foster a collaborative, patient-centric, and results-driven culture. Ensure appropriate training, learning, and personal development opportunities for all team members. Establish and maintain a positive and motivating working environment. Role model Cytokinetics´ company values. Sales &amp; Market Strategy Execution Develop and execute a strategic regional business plan aligned with national objectives, in close collaboration with the DACH Leadership Team. Define and implement segmentation and targeting strategies for key local prescriber groups. Co-establish sales objectives with country leadership by forecasting and setting annual quotas, projecting sales volumes and market shares for existing and new products. Monitor regional performance against targets, analyze gaps, and adjust strategies proactively. Implement and oversee the rollout of CRM systems and tools to support sales effectiveness. Market &amp; Customer Engagement Build and maintain strong relationships with Key Opinion Leaders (KOLs), healthcare professionals (HCPs), and key accounts. Educate providers on the clinical benefits and appropriate use of the company’s therapies. Collaborate cross-functionally with medical, market access, and marketing teams to ensure aligned customer engagement and product support. Develop and implement account action plans to drive in-label usage of approved products within the appropriate patient populations. Compliance &amp; Operational Excellence Ensure full adherence to regulatory, legal, and compliance standards. Promote ethical sales practices and maintain accurate documentation. Monitor competitive trends and market dynamics, adjusting strategies as needed. Complete operational requirements by scheduling and assigning responsibilities and following up on execution and results. QUALIFICATIONS AND EXPERIENCE Educational Background Bachelor’s degree required; advanced degree in Life Sciences or an MBA is preferred. Industry Experience Minimum of 10 years of experience in the pharmaceutical or biotechnology industry in field-based sales roles. At least 2 years of proven success in sales leadership, ideally in regional management within smaller, agile team environments. Demonstrated experience in product launches and driving regional sales growth. Experience in specialized cardiology indications would be beneficial, but not a requirement. Skills &amp; Attributes Strong leadership, coaching, and team-building capabilities. Strategic thinker with solid business acumen and the ability to develop and execute regional sales strategies. Excellent communication, negotiation, and analytical skills. Creative, curious, and solutions-oriented with a hands-on, can-do attitude. Comfortable advocating for the value and pricing of innovative pharmaceutical products. Proficiency in Microsoft Office Suite and CRM tools. Language &amp; Communication Business fluency in German and a high level of proficiency in English are required. Travel &amp; Location Willingness and ability to travel extensively (up to 65%) across large territories; this is a 100% field-based role. What We Offer The privilege to participate in building and shaping the in-country operations of an exciting, dynamic company in the DACH region, assuming personal responsibility for business-critical projects and processes within a team of highly experienced professionals. An opportunity to join a scientifically outstanding, research-based specialty care pharmaceutical company, shaping the future of innovative treatments in muscle biology. A highly collaborative and inclusive environment which supports professional growth and personal development. A very competitive salary and benefits package above industry average. &nbsp; &nbsp; &nbsp;Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Regional Sales Manager

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Cytokinetics is seeking a highly experienced Senior Director, Commercial Regulatory Affairs and Business Operations, to join the Regulatory Affairs team in Europe. They will play a key role in ensuring that all promotional materials and activities comply with regional and local regulatory requirements, aligning with the company's commercial objectives. This role is also pivotal in ensuring the efficient and compliant operation of our regulatory affairs department, with a focus on collaborating with the general managers and regulatory local vendors across our affiliates in Europe. They will help develop the infrastructure of the Regulatory Affairs Department in Europe, including implementation of process improvements to enhance the efficiency of operations as well as oversight of regulatory policy changes in Europe and their impact on business operations.The ideal candidate will possess a strong experience and understanding of regulatory requirements and processes related to promotion and commercialization, excellent organizational skills, and the ability to work effectively with cross-functional teams to streamline operations and support business objectives.Responsibilities Advertising and promotional activities: Lead and manage the European MLR process, ensuring timely and compliant regulatory review of promotional and non-promotional materials in Europe. Training and Guidance: Provide training and guidance to internal teams on regulatory requirements and best practices for promotional activities and other activities as required. Oversight of local regulatory activities: Develop and oversee the local regulatory activities through vendor selection, management and serve as the primary liaison between the central regulatory affairs team and local regulatory vendors, ensuring alignment of regulatory strategies and objectives. Cross-Functional Collaboration: Work closely with internal departments, including Pharmacovigilance, Quality Assurance, Commercial and Medical teams, to ensure regulatory activities are conducted timely and compliantly. Regulatory Compliance: Ensure all regulatory activities are conducted in compliance with applicable regulations and guidelines, maintaining up-to-date knowledge of regulatory requirements in each country’s jurisdiction. Standard Operations Procedures development: work cross functionally to ensure all relevant regulatory SOPs at regional and local levels are in place. Budget management: Help manage and coordinate budget of the regulatory department in Europe and provides input into budgeting and resource requirements. Process Improvement: Identify opportunities for process enhancements within the regulatory affairs function to increase efficiency and compliance. Regulatory Intelligence: Oversee the regulatory policy requirements changes in Europe and ensure timely communication of impacts to relevant stakeholders. Qualifications Seasoned professional with a minimum of 12 years of relevant experience with solid expertise and knowledge of the applicable European regulatory regulations, directives and guidelines Strong experience understanding of European regulatory requirements, particularly concerning promotional activities. Prior experience in advertising and promotion regulatory roles is a must. Must have experience dealing with regulatory representatives in the EU countries. Must have solid understanding of quality and GxP standards. Excellent communication and leadership skills. Ability to work effectively in a cross-functional, matrixed environment. Must be a strong team player, a fully engaged, hands-on professional capable of working collaboratively and independently, with excellent verbal and written communication skills. Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects. Strong interpersonal capabilities and ability to build and maintain networks. Possesses sense of urgency; identifies challenges and problems and takes the initiative to identify solutions. Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Senior Director, Commercial Regulatory Affairs and Business Operations - Europe

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. The Inventory and Operations Manager is responsible for overseeing the execution of processes that support the manufacturing and movement of pharmaceutical products throughout the value chain. This role ensures accurate inventory management across the supply network and plays a crucial role in facilitating timely transactional activities, including goods receipts, issues, and product movements. As a key Subject Matter Expert (SME) in Planning &amp; Inventory Operations, the manager leads the design and development of processes, creating process maps, process design documentation, and training materials. Additionally, they serve as stewards of master data, actively managing and promoting Master Data Management practices to ensure data integrity across the supply chain. Key Responsibilities Process Execution and Data Stewardship Work with suppliers, manufacturers, and third-party logistics providers to ensure timely and efficient execution of supply chain transactions across the value chain Perform goods receipts, goods issues, transfers, and other goods movements in support of Supply Execution at external suppliers, warehouses and distribution centers Works closely with the Quality team to ensure accurate product status for all inventory at third-party sites and assists in resolving any related issues Conducts regular inventory audits and reconciles discrepancies between physical stock and records Works closely with the Finance team to ensure accurate and correct inventory valuation throughout the value chain Collaborates closely with Procurement and Logistics on status on inbound and outbound material and product inventory Partners with the Planning team on product demand and scenario planning to manage inventory Serves as the steward for Master Data Management supporting the flawless execution of Supply Chain process execution for inventory management Process Subject Matter Expert (SME) Oversee the end-to-end pharmaceutical supply chain process design as a key Subject Matter Expert (SME), across the Value Chain for inventory management Develop Process Maps, Process Documentation, and Training materials supporting execution across Value Chain inventory processes Create and own user training and development documentation supporting end user execution and ensure all users are trained and knowledgeable of all value chain inventory processes Regulatory Compliance &amp; Documentation: Ensure adherence to pharmaceutical industry regulations, including Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), and other relevant compliance standards Maintain accurate and up-to-date records for all inventory transactions, including receipts, shipments, and goods movements Performance Reporting and Analysis: Develop and maintain key performance indicators (KPIs) to assess inventory accuracy and management, and process performance across the value chain Identify and implement process improvements to streamline inventory and supply chain operation to help ensure inventory availability, reduce costs and enhance customer satisfaction Continuous Improvement: Evaluate current processes and identify opportunities for improvement in supply chain and inventory management practices Stay current with industry trends, technologies, and best practices to continually enhance supply chain efficiency and inventory control Qualifications Bachelor’s degree in Supply Chain Management, Industrial Engineering, Business Administration, or a related field Master’s degree or MBA preferred, with additional certifications in supply chain (e.g., APICS, Six Sigma, PMP) Minimum 5+ years of experience in supply chain, inventory management, or supply operations within the pharmaceutical or healthcare industry Experience working with supply chain management software and ERP systems (e.g., Oracle, SAP, or similar) Familiarity with pharmaceutical supply chain regulations and industry best practices Ability to work under pressure, manage competing priorities, and meet deadlines Strong attention to detail and commitment to maintaining high-quality standards Ability to travel as required to support inventory management processes and audits Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Senior Manager Supply Chain Inventory and Operations

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Dans le cadre de l’implantation et du développement de la filiale française de Cytokinetics, le Pharmacien Responsable / Directeur des Affaires Pharmaceutiques est chargé de poser les fondations réglementaires, qualité, pharmacovigilance et conformité pour les activités locales. Rattachée à la Directrice Générale France &amp; Benelux, avec un lien fonctionnel à la Directrice Europe des Affaires Réglementaires, vous piloterez&nbsp;la constitution du dossier d’ouverture/obtention du statut d’exploitant&nbsp;auprès de l’ANSM, la mise en place du Système de Gestion de la Qualité (QMS/PQS)&nbsp;local, la rédaction et le déploiement des SOP&nbsp;locales, ainsi que l’intégration des systèmes d’Information Médicale&nbsp;et de gestion documentaire. Vous assurerez en parallèle toutes les responsabilités réglementaires classiques (AMM, labelling, pharmacovigilance, conformité, relation autorités) et jouerez un rôle clé dans la gestion des audits et inspections, la supervision des pratiques promotionnelles (charte de l’information, charte de la visite médicale) et le contrôle des supports de visite médicale. Vous serez l’interlocuteur central entre le siège EU, le global et les autorités sanitaires françaises pour garantir la conformité locale et soutenir le lancement, la maintenance et l’évolution des produits, tout en représentant Cytokinetics au sein des instances professionnelles comme le LEEM et l’IFIS. Responsabilités &amp; périmètre d’action Élaborer et piloter le dossier d’ouverture / demande de statut d’exploitant auprès de l’ANSM (organisation, justificatifs, documents techniques, conformité réglementaire). Définir, structurer et déployer un Qualité Management System local (PQS / QMS) : politique qualité, organigramme qualité, maîtrise documentaire, change control, gestion des déviations et CAPA, audits internes, management des fournisseurs, plan de formation et préparation des inspections. Rédiger, valider, déployer et mettre à jour les SOPs locales couvrant les domaines essentiels : pharmacovigilance, réclamations produits, rappels / retraits, transport et stockage GDP, gestion des prestataires, information médicale, promotion, formation, documentation. Piloter et superviser les activités réglementaires locales : AMM / variations, labelling / notice en français, suivi réglementaire, interactions avec l’ANSM et les autorités européennes. Mettre en place et gérer la pharmacovigilance locale en coordination avec l’équipe EU PV : gestion des cas, signal détection, PGR, audits GVP et suivi des prestataires. Superviser le service d’information médicale : mise en place du processus, supervision des réponses aux demandes scientifiques, validation des FAQ standards, coordination avec le département médical EU / Global. Être un acteur clé des audits et inspections (ANSM, internes, prestataires) : préparation, accueil des inspecteurs, réponses CAPA, suivi des actions correctives et amélioration continue. Veiller à la conformité des activités de visite médicale / information promotionnelle, en application de la Charte de l’Information Promotionnelle / Charte de la Visite Médicale (LEEM) : validation et contrôle des supports, suivi de la traçabilité, formation des délégués, conformité au référentiel IFIS et obligations légales. Interagir activement avec les organismes professionnels externes (LEEM, IFIS) pour le suivi réglementaire, la participation aux groupes de travail sectoriels, la mise à jour des chartes, la veille éthique et le maintien des certifications. Assurer le pilotage transversal avec les départements Médical Affairs, Market Access, Commercial, Supply Chain, Réglementaire et Legal pour garantir la conformité des activités, des supports et des communications produits. Superviser la mise en place et le pilotage de programmes d’accès précoces tout en collaborant étroitement avec les équipes globales (Développement clinique, R&amp;D, Affaires Médicales, Market Access, Réglementaire) et en gérant les interactions avec les acteurs externes (ANSM, médecins &amp; pharmaciens hospitaliers) Manager et superviser les prestataires externes (consultants qualité/réglementaire, QP externes, logistique, distribution) impliqués dans les activités locales. Mettre en place les reportings de conformité locale (KPI qualité, audits, incidents, CAPA, pharmacovigilance, préparation de l’inspection) vers la direction France et Europe. Veiller à la formation continue et à la compétence des collaborateurs sur les bonnes pratiques réglementaires, de pharmacovigilance, qualité et information médicale. Profil recherché Nos équipes rassemblent des profils variés et nous valorisons ces différences. Nous recherchons les meilleurs talents pour nos postes ouverts, mais il n’est pas nécessaire de répondre à 100 % des critères pour que votre candidature soit étudiée. Si ce que vous pourriez accomplir chez Cytokinetics vous enthousiasme et si vous pensez pouvoir apporter de la valeur à notre équipe, nous serions ravis de recevoir votre candidature Diplôme de licence (Bac+3) ou expérience professionnelle équivalente Au moins 2 ans d’expérience pertinente dans l’industrie pharmaceutique (poste de coordinateur/trice ou de gestion de projet) souhaités Maîtrise de l’anglais indispensable ; la connaissance d’autres langues de l’UE est un atout Expérience avérée dans la gestion simultanée de plusieurs projets Excellentes compétences de saisie, maîtrise de Microsoft Office ; expérience des systèmes électroniques de gestion/contrôle documentaire (EDMS) Excellentes compétences en communication, résolution de problèmes et sens du détail Solides aptitudes interpersonnelles, esprit d’équipe, sens de l’organisation et de la planification de la charge de travail Capacité à travailler de manière autonome et à prendre des initiatives Aptitude à développer et entretenir des relations efficaces ; aisance avec des interlocuteurs de profils variés et dans des contextes différents ; forte orientation client (écoute, courtoisie, tact, empathie, attention). Ce que nous offrons Un rôle clé dans la construction de la filiale française et la préparation des lancements. Une large autonomie de décision dans un environnement biotech innovant à fort impact scientifique. Une structure agile et une équipe en construction dynamique. #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Pharmacien Responsible/ Directeur des Affaires Pharmaceutiques

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. The Global Supply Planner (Contract) will support the Commercial Supply Chain team in executing end-to-end (E2E) tactical supply planning activities for an assigned brand portfolio. This role focuses on coordinating demand, supply, and inventory plans across Supply Chain (SC) nodes, maintaining accurate planning data, and ensuring seamless alignment across cross-functional teams. The position will contribute to the monthly planning cycle, including demand propagation to bulk production and Drug Substance/API. Key Responsibilities End to End Supply Planning Execution Support the development and maintenance of global supply plans, ensuring alignment with business requirements, regulatory standards, and market needs. Help optimize inventory strategies and E2E supply chain configurations by maintaining accurate planning parameters and identifying potential risks. Execute planning activities in compliance with pharmaceutical regulations and internal SOPs. Sales &amp; Operations Planning (S&amp;OP) Support Prepare data, analyses, and scenario models to support the S&amp;OP process. Collaborate with cross-functional partners to review demand, supply, and inventory positions and highlight potential imbalances. Assist in resolving supply disruptions, capacity constraints, and forecast discrepancies by providing analysis and recommendations. Budget &amp; Performance Planning Support Contribute to the creation of supply plans used for annual budget processes, including capacity, inventory, and purchasing inputs. Track and report operational KPIs such as service levels, inventory levels, on-time delivery performance, and forecast accuracy. Support the balance of short-term operational needs with longer-term planning considerations. Cross-Functional Collaboration Partner with teams including regulatory affairs, quality, commercial, finance, external manufacturing, and logistics to ensure alignment of supply plans. Provide planning insights to internal stakeholders and ensure coordinated execution of supply chain activities. Work with regional and local teams to support regulatory- and market-specific requirements. Continuous Improvement &amp; Innovation Participate in initiatives to streamline planning processes and enhance operational efficiency. Monitor industry trends, technologies, and regulatory updates relevant to supply planning. Support implementation of planning system enhancements and best practices. Qualifications Bachelor’s degree in Supply Chain Management, Pharmaceutical Sciences, Business Administration, or a related field. 7–10 years of experience in pharmaceutical supply chain or related planning functions. Strong understanding of pharmaceutical production processes, inventory management, and regulatory requirements (GxP, FDA, EMA). Experience with supply chain systems and planning tools (e.g., ERP, forecasting software). Excellent analytical, problem-solving, and data-driven decision-making skills. Strong communication and interpersonal skills with the ability to work effectively across cross-functional teams. Prior experience in the pharmaceutical or life sciences industry with exposure to global supply chain operations. #LI-HYBRID &nbsp;Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Contract - Global Supply Planner

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.The&nbsp;Regional Sales Manager, South Germany leads a high-performing team to drive growth across the region, with a strong focus on strategic execution, customer engagement, and cross-functional collaboration. This role is responsible for developing and executing business plans, cultivating relationships with key healthcare professionals, ensuring regulatory compliance, and fostering a results-oriented, patient-centric culture. This is a senior-level commercial leadership position within the pharmaceutical (biotech) industry, ideally suited for someone who thrives on high-level scientific exchange and finds purpose in bringing first-in-class treatments to patients—positively impacting their lives and those of their families. The Regional Sales Manager will lead a team of dedicated Key Account Managers within the assigned region. The role offers a high degree of autonomy and visibility, along with a unique opportunity to shape how Cytokinetics is positioned in the DACH region. &nbsp; ROLE RESPONSIBILITIES Leadership &amp; Team Development Recruit, lead, coach, and mentor a high-performing team of Key Account Managers. Conduct regular field visits and coaching sessions to ensure effective sales execution. Set and monitor individual and team goals, including incentive plans and development objectives. Foster a collaborative, patient-centric, and results-driven culture. Ensure appropriate training, learning, and personal development opportunities for all team members. Establish and maintain a positive and motivating working environment. Role model Cytokinetics´ company values. Sales &amp; Market Strategy Execution Develop and execute a strategic regional business plan aligned with national objectives, in close collaboration with the DACH Leadership Team. Define and implement segmentation and targeting strategies for key local prescriber groups. Co-establish sales objectives with country leadership by forecasting and setting annual quotas, projecting sales volumes and market shares for existing and new products. Monitor regional performance against targets, analyze gaps, and adjust strategies proactively. Implement and oversee the rollout of CRM systems and tools to support sales effectiveness. Market &amp; Customer Engagement Build and maintain strong relationships with Key Opinion Leaders (KOLs), healthcare professionals (HCPs), and key accounts. Educate providers on the clinical benefits and appropriate use of the company’s therapies. Collaborate cross-functionally with medical, market access, and marketing teams to ensure aligned customer engagement and product support. Develop and implement account action plans to drive in-label usage of approved products within the appropriate patient populations. Compliance &amp; Operational Excellence Ensure full adherence to regulatory, legal, and compliance standards. Promote ethical sales practices and maintain accurate documentation. Monitor competitive trends and market dynamics, adjusting strategies as needed. Complete operational requirements by scheduling and assigning responsibilities, and following up on execution and results. &nbsp;QUALIFICATIONS AND EXPERIENCE Educational Background Bachelor’s degree required; advanced degree in Life Sciences or an MBA is preferred. Industry Experience Minimum of 10 years of experience in the pharmaceutical or biotechnology industry in field-based sales roles. At least 2 years of proven success in sales leadership, ideally in regional management within smaller, agile team environments. Demonstrated experience in product launches and driving regional sales growth. Experience in specialized cardiology indications would be beneficial, but not a requirement. Skills &amp; Attributes Strong leadership, coaching, and team-building capabilities. Strategic thinker with solid business acumen and the ability to develop and execute regional sales strategies. Excellent communication, negotiation, and analytical skills. Creative, curious, and solutions-oriented with a hands-on, can-do attitude. Comfortable advocating for the value and pricing of innovative pharmaceutical products. Proficiency in Microsoft Office Suite and CRM tools. Language &amp; Communication Business fluency in German and a high level of proficiency in English are required. Travel &amp; Location Willingness and ability to travel extensively (up to 65%) across large territories; this is a 100% field-based role. What We Offer The privilege to participate in building and shaping the in-country operations of a young, dynamic company in the DACH region, assuming personal responsibility for business-critical projects and processes within a team of highly experienced professionals. An opportunity to join a scientifically outstanding, research-based specialty care pharmaceutical company, shaping the future of innovative treatments in muscle biology. A highly collaborative and inclusive environment which supports professional growth and personal development. A very competitive salary and benefits package above industry average. Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Regional Sales Manager, South Germany

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. Own the end‑to‑end technical enablement of Drug Substance (API) supply for Aficamten across an external CMO network. Deliver robust technology transfer, scale‑up and PPQ readiness, commercial control strategy and ongoing CPV to ensure reliable, compliant and cost‑effective supply. Drive process robustness, investigations and continuous improvement, and serve as the primary technical interface to CMO’s.Operate cross‑functionally: provide data packages and technical summaries in partnership with Regulatory/ CMC, QA&amp;C, and Supply Chain. Lead the technical plan for dual‑sourcing (API/critical starting materials) and hand over filing/quality/commercial actions to the owning functions. Responsibilities External Manufacturing / Technical Operations Lead onboarding, and technical oversight of CMOs for Drug Substance; input to MSAs, SoWs and KPIs. Dual‑sourcing – technical enablement: Lead the technical plan to qualify an alternate API/RSM /KSM source—process &amp; method transfer, engineering runs and PPQ readiness, comparability/CPV set‑up—in partnership with Reg CMC (filings/variations), QA&amp;C (audits/release), and Supply Chain (commercials/capacity). Own tech transfer, scale‑up, PPQ strategy and execution; define/maintain the commercial control strategy and CPV plan. Drive process robustness and continuous improvement at partners; lead/coach investigations (deviations/OOS/OOT) to root cause. Process &amp; Scientific Leadership Own synthetic route and process optimization; set CPPs/CMAs, impurity control strategy, and DS specifications. Define raw‑material strategy (critical starting materials) and second‑source technical requirements. Regulatory CMC (Drug Substance) Partner with Reg CMC by providing technical data, comparability and PPQ summaries to support site‑addition variations and lifecycle updates. Reg CMC owns dossier authorship/submission and Health Authority interactions (queries, approvals). Quality &amp; Compliance (with QA) Partner with QA&amp;C to supply technical inputs for audits/PAI readiness and to close technical actions from deviations/CAPAs. &nbsp;QA&amp;C owns Quality Agreements, external audits, product release/COA, and QMS governance. Supply, Cost &amp; Risk Partner with External Supply / Supply Chain on supplier selection, contracts, campaign planning and inventory/safety‑stock strategy; provide the technical plan and readiness dates. External Supply / Supply Chain owns commercial budget, capacity and the master supply risk register; Tech Ops owns the technical risk register and mitigations. Analytics / Data &amp; Ways of Working Establish dashboards for yield/throughput/Right‑First‑Time/OTIF/CoGs; trend process and CPV data from CMOs. Lead cross‑functional routines and governance with internal stakeholders and partners. Qualifications Education &amp; Core Experience MSc/PhD in Chemical Engineering, Organic/Process Chemistry (or related). 15+ years in small-molecule API from late-stage development to commercial manufacturing with CMOs. Proven leadership of tech transfer, scale-up, PPQ, commercial control strategy, and CPV for API. Technical Depth Strong GMP and ICH Q7, Q8–Q12 working knowledge. Demonstrated process robustness: CPP/CMA definition, impurity control, specification setting, and raw-material/CSM strategy. Hands-on investigations/RCA (OOS/OOT/deviations) and continuous improvement at external sites. &nbsp;Comfortable with statistics/DoE/SPC and data trending for CPV. Cross-Functional Interfaces (scope clarity) Regulatory CMC: Generate high-quality technical content/data packages (comparability, PPQ summaries) and respond to HA queries; Reg CMC owns dossiers &amp; submissions. QA&amp;C: Provide technical inputs to audits/PAI readiness and CAPAs; QA&amp;C owns QAA, release, and QMS. External Supply / Supply Chain: Provide the technical plan and readiness dates; they own commercials, capacity, and the master supply risk register Vendor &amp; Network Leadership CMO governance (KPIs, SoWs), performance management, and second-source technical enablement experience (preferred). Plus Factors Early-career on-plant API/DS manufacturing exposure (strong plus). Prior site-addition / dual-sourcing technical packages; solvent recovery/cost-down achievements. Multi-region experience (US/EU/ICH), additional European language(s). Ways of Working Crisp technical writing; influence without authority; decisive, data-driven; comfortable with 25 – 30% travel. #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Director, Technical Operations API

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Reporting directly to the&nbsp;Director Market Access, DACH, the Field Market Access Manager, West Germany is responsible for executing market access strategies within an assigned region&nbsp;to ensure optimal patient access to therapies. Working closely with the Director Market Access DACH and cross-functional teams (Sales, Marketing, Medical), the role focuses on: Implementing regional pricing and reimbursement tactics, engaging with local payers and healthcare stakeholders, addressing access barriers at hospital and office-based account level in cardiology care. The Field Market Access Manager contributes to regional insights and data analysis, tactical solutions to support successful reimbursement outcomes, strategic input to align local execution with the broader commercial objectives. This role requires strong stakeholder engagement skills, a deep understanding of regional healthcare dynamics, and the ability to operate independently while collaborating proactively across functions. ROLE RESPONSIBILITIES Stakeholder Engagement and Relationship Management Support commercial Key Account Managers with face-to-face, personal and individual HCP education on regional and local reimbursement regulations in order address questions regarding funding of high-value specialty care medicines in cardiology. Build and maintain strong relationships with regional payers, sick funds, SHI physicians’ associations, hospital controllers, retail pharmacists, and other healthcare decision-makers. Engage with drug evaluation committees and payer organizations to facilitate patient access and reduce funding barriers. Represent the company in compliant interactions, offering value-added solutions to support access and reimbursement. Cross-functional Collaboration Visit HCPs together with commercial Key Account Managers, on a regular basis Collaborate closely with Sales, Marketing, Medical and other internal teams to align on access priorities and ensure coordinated execution. Contribute to cross-functional projects that enhance regional access and create win-win solutions with stakeholders. Provide tools, training, and insights to support field teams in overcoming market access barriers and pricing concerns of HCPs. Data, Insights &amp; Policy Monitoring Monitor and analyze regional healthcare developments, policy changes, and reimbursement trends. Collect and interpret local data to inform strategic planning and tactical execution. Share insights with internal teams to optimize market access approaches and anticipate challenges. Communication &amp; Training Develop and deliver training presentations for sales teams and external stakeholders on relevant health policy, pricing, and reimbursement topics, tailored to specialty cardiology issues. Create and adapt materials that communicate the value of innovative specialty care products in a way that resonates with regional stakeholders. Present complex market access topics in a clear, audience-appropriate format at internal and external events. Project &amp; Event Management Plan, manage, and monitor regional projects, including contracts and agreements with payers, in coordination with the DACH Management Team. Organize and lead access-related events such as expert meetings, roundtables, and commercial meetings in both hospital and outpatient settings. Use both digital and analogue channels to engage with stakeholders and support collaboration. QUALIFICATIONS AND EXPERIENCE Educational Background A bachelor’s degree is required; an advanced university degree is preferred—ideally in natural sciences, healthcare-related fields, economics or business administration. Additional qualifications in health economics, health policy, or market access are considered a strong asset. Industry Experience Minimum of 5 years of professional experience in the pharmaceutical or biopharmaceutical industry, with a focus on market access, health policy, or reimbursement. At least 2 years of hands-on experience in regional market access or related field-based roles, with a proven track record of executing access strategies operatively at the customer level. Healthcare System Expertise In-depth knowledge of the German healthcare system and self-administration structures, including legal frameworks for pricing and reimbursement in both outpatient and inpatient sectors. A resilient network of regional stakeholders within the German healthcare system, particularly with sick funds and payor bodies. Stakeholder Management and Communication Demonstrated success in stakeholder engagement, with the ability to build and maintain influential networks across regional healthcare institutions. Strong communication and presentation skills, with the ability to convey complex healthcare and policy topics in a clear, audience-appropriate and convincing manner. High motivation, goal orientation, and a collaborative yet independent working style. Cross-functional and Digital Competence Experience working in matrixed, fast-paced environments and managing cross-functional projects. Excellent project management skills, with the ability to handle multiple complex initiatives simultaneously and deliver results on time. IT-savvy, with proficiency in modern digital communication tools and MS Office applications Strategic &amp; Analytical Thinking Strong analytical and strategic thinking capabilities, with a passion for translating complex interrelationships into actionable insights. Interest in health policy developments and their impact on market access and reimbursement. Language and Travel Native-level fluency in German and business-fluent English, both written and spoken. Willingness to travel regularly across the assigned region and the broader DACH area, including frequent overnight trips.&nbsp; #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Field Market Access Manager, West Germany

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. Reporting to the Executive Director, Regulatory Affairs - CMC, the Director of Regulatory Affairs-CMC is responsible for leading regulatory support for assigned programs to ensure sound regulatory planning and tactical implementation of US and international regulatory submission strategies. Responsibilities Formulate CMC regulatory strategies, without supervisor oversight, based on current regulatory intelligence. Collaborates with cross-functional project teams and external business partners to develop CMC regulatory strategies and identify regulatory risks; represents the department in cross-functional project teams. Identifies the required documentation and any content, quality and timeline issues for global submissions and manages the delivery of approved technical documents in accordance with project timelines. Manages the preparation, authoring and maintenance of regulatory submission documents pertaining to CMC data for global clinical trial and marketing applications, as well as post-marketing variations. May require technical regulatory authoring of submission package components. Supports the evaluation of manufacturing changes for the potential impact on products. Provides expert review of CMC documentation supporting regulatory submissions and communications. Coordinates preparation of responses to queries from regulatory authorities, particularly focused on CMC. May require technical regulatory authoring to support responses to queries. Maintains knowledge and expertise with FDA/EMA regulations, ICH guidelines and other international regulatory regulations and guidelines, as needed to support global programs. Ensures conformance to commitments made with various regulatory agencies (e.g., IND/CTA commitments) for assigned programs. Provides regulatory advice to other functional areas. May participate in regulatory due diligence activities. Relationships Build and maintain collaborative relationships with internal/external business partners to achieve project regulatory goals. Develops and maintains collaborative relationships with other departments to ensure effective communication regarding project regulatory goals, issues and timelines. Develop and manage relationships with external vendors and regulatory health authorities. Coordinates activities for meetings and conferences with FDA, EMA, and other regulatory authorities Collaborate with regulatory colleagues to provide CMC expertise as needed. Management This is an Individual Contributor position; however, there is the possibility for supervising consultants/contractors and/or interns. Develops and implements regulatory operating guidelines and common work practices/strategies within the team. Qualifications 10 - 12+ years of related work experience (Director candidates will typically bring 12+ years; Associate level candidates may be considered with 10+ years and strong potential), including 8+ years in Regulatory Affairs CMC in the Biotech/Pharmaceutical industry; experience in small molecule drug development required; experience in the cardiovascular therapeutic area is a plus Proven experience serving as a primary RA-CMC contact to Health Authorities, with full strategic responsibility. Bachelor’s degree is required, preferably in chemistry or a closely related field; advanced degree is a plus. Advanced degree is preferred. Excellent working knowledge of international regulatory requirements and environment, including an understanding of GXP Solid working knowledge of core processes associated with discovery, development, and manufacturing of small molecules. Experience with eCTD requirements and electronic submissions Experience with international regulatory submissions and processes is a strong plus. Ability to work effectively across teams, functions and with outside partners. Excellent oral and written communication skills Excellent organizational skills and attention to detail Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Reporting directly to the&nbsp;Director Market Access, DACH, the&nbsp;Field Market Access Manager&nbsp;is responsible for executing market access strategies within an assigned region—such as&nbsp;Northern or Southern Germany—to ensure optimal patient access to therapies. Working closely with the Director Market Access DACH and cross-functional teams (Sales, Marketing, Medical), the role focuses on: Implementing regional pricing and reimbursement tactics, engaging with local payers and healthcare stakeholders, addressing access barriers at hospital and office-based account level in cardiology care. The Field Market Access Manager contributes to regional insights and data analysis, tactical solutions to support successful reimbursement outcomes, strategic input to align local execution with the broader commercial objectives. This role requires strong stakeholder engagement skills, a deep understanding of regional healthcare dynamics, and the ability to operate independently while collaborating proactively across functions. ROLE RESPONSIBILITIES Stakeholder Engagement and Relationship Management Support commercial Key Account Managers with face-to-face, personal and individual HCP education on regional and local reimbursement regulations in order address questions regarding funding of high-value specialty care medicines in cardiology. Build and maintain strong relationships with regional payers, sick funds, SHI physicians’ associations, hospital controllers, retail pharmacists, and other healthcare decision-makers. Engage with drug evaluation committees and payer organizations to facilitate patient access and reduce funding barriers. Represent the company in compliant interactions, offering value-added solutions to support access and reimbursement. Cross-functional Collaboration Visit HCPs together with commercial Key Account Managers, on a regular basis Collaborate closely with Sales, Marketing, Medical and other internal teams to align on access priorities and ensure coordinated execution. Contribute to cross-functional projects that enhance regional access and create win-win solutions with stakeholders. Provide tools, training, and insights to support field teams in overcoming market access barriers and pricing concerns of HCPs. Data, Insights &amp; Policy Monitoring Monitor and analyze regional healthcare developments, policy changes, and reimbursement trends. Collect and interpret local data to inform strategic planning and tactical execution. Share insights with internal teams to optimize market access approaches and anticipate challenges. Communication &amp; Training Develop and deliver training presentations for sales teams and external stakeholders on relevant health policy, pricing, and reimbursement topics, tailored to specialty cardiology issues. Create and adapt materials that communicate the value of innovative specialty care products in a way that resonates with regional stakeholders. Present complex market access topics in a clear, audience-appropriate format at internal and external events. Project &amp; Event Management Plan, manage, and monitor regional projects, including contracts and agreements with payers, in coordination with the DACH Management Team. Organize and lead access-related events such as expert meetings, roundtables, and commercial meetings in both hospital and outpatient settings. Use both digital and analogue channels to engage with stakeholders and support collaboration. QUALIFICATIONS AND EXPERIENCE Educational Background A bachelor’s degree is required; an advanced university degree is preferred—ideally in natural sciences, healthcare-related fields, economics or business administration. Additional qualifications in health economics, health policy, or market access are considered a strong asset. Industry Experience Minimum of 5 years of professional experience in the pharmaceutical or biopharmaceutical industry, with a focus on market access, health policy, or reimbursement. At least 2 years of hands-on experience in regional market access or related field-based roles, with a proven track record of executing access strategies operatively at the customer level. Healthcare System Expertise In-depth knowledge of the German healthcare system and self-administration structures, including legal frameworks for pricing and reimbursement in both outpatient and inpatient sectors. A resilient network of regional stakeholders within the German healthcare system, particularly with sick funds and payor bodies. Stakeholder Management and Communication Demonstrated success in stakeholder engagement, with the ability to build and maintain influential networks across regional healthcare institutions. Strong communication and presentation skills, with the ability to convey complex healthcare and policy topics in a clear, audience-appropriate and convincing manner. High motivation, goal orientation, and a collaborative yet independent working style. Cross-functional and Digital Competence Experience working in matrixed, fast-paced environments and managing cross-functional projects. Excellent project management skills, with the ability to handle multiple complex initiatives simultaneously and deliver results on time. IT-savvy, with proficiency in modern digital communication tools and MS Office applications Strategic &amp; Analytical Thinking Strong analytical and strategic thinking capabilities, with a passion for translating complex interrelationships into actionable insights. Interest in health policy developments and their impact on market access and reimbursement. Language and Travel Native-level fluency in German and business-fluent English, both written and spoken. Willingness to travel regularly across the assigned region and the broader DACH area, including frequent overnight trips.&nbsp; Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Field Market Access Manager, DACH

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM), Baden-Württemberg, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Baden-Württemberg

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM), Berlin, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Berlin

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM), Brandenburg, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Brandenburg

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM), Bremen, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Bremen

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM), Hessen, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Hessen

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM), Mecklenburg-Vorpommern, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Mecklenburg-Vorpommern

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM), Nordrhein-Westfalen, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Nordrhein-Westfalen

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM), Niedersachsen, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Niedersachsen

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM),&nbsp;Rheinland-Pfalz, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Rheinland-Pfalz

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM), Sachsen-Anhalt, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Sachsen-Anhalt

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM), Schleswig-Holstein, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Schleswig-Holstein

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.The Sales and Marketing Coordinator plays a vital cross-functional role within the DACH Commercial Department, reporting directly to the Commercial Director DACH. This position supports the efficient planning and execution of key sales and marketing activities, serving as an operational backbone to the Commercial Team. Acting as a crucial interface between the Commercial Director, Product Managers, external agencies, and internal stakeholders (including Medical Affairs, Legal, and Procurement), the role ensures the timely coordination and implementation of promotional materials, sponsorships, and event logistics. A key responsibility is managing the required contracting and approval processes, e.g. MLR approval process and handling the submission and tracking of materials via Veeva PromoMats, as well as external vendor contracts, for example sponsorship and speaker engagements in Germany. The ideal candidate brings structure, diligence, compliance awareness, and executional excellence to the day-to-day commercial operations, contributing directly to the successful implementation of marketing initiatives and sales support activities. Attention to detail, proactive communication, and efficient, reliable process coordination are essential for success in this role. Responsibilities Project Coordination &amp; Operational Support: Coordination of sponsorship agreements and other contract requests. Support for event and meeting planning, including venue and material coordination. Manage healthcare professional (HCP) events such as congresses, symposia, educational meetings, and expert panels in collaboration with Commercial and Medical Affairs teams. Independently manage and track requests related to promotional and scientific events. Interface with external vendors, creative agencies, and internal teams. Administration of OPEX budget tracking tools and reports. Material Review, approval and production: Coordination of promotional material submissions and (re)approvals in Veeva PromoMats. MLR review process support and follow-up. Ensure compliance with internal SOPs and industry regulations during the approval process. Coordinate and supervise timely production of marketing materials with external vendors. Contract and Vendor Management: Initiate and track contracts including sponsorships and service agreements. Collaborate with procurement to manage Purchase Orders, invoices, and supplier onboarding in collaboration with the Finance / Procurement Team. Maintain clear communication with agencies and print service providers for materials and campaigns, ensuring timelines and agreements are adhered to. Documentation &amp; Compliance: Support updating marketing of material libraries, including upload to Veeva Vault and SharePoint. Ensure timely follow-up for certifications and re-approvals of promotional materials. Qualifications and personal skills: Bachelor's degree in Business Administration or Equivalent degree &amp; proven experience in pharmaceutical marketing or sales coordination roles. At least 5 years of experience in comparable roles within the pharmaceutical industry Solid understanding of German pharmaceutical compliance regulations. Operative experience with Veeva PromoMats and MLR processes. Strong project management, organization, and communication skills. Advanced proficiency with office software (e.g. Office 365), administrative/finance tools, and contract management systems. Fluency in German and English (written and spoken). Ability to handle multiple stakeholders and prioritize tasks effectively. Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Sales & Marketing Coordinator, DACH

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Our passion is anchored in our four core values: Patients are our North Star: Our actions and decisions are dedicated to benefiting patients and their caregivers. Science is in our Soul: We are committed to scientific excellence, integrity, and critical thinking, free from external influences. We &gt; Me: Our strength lies in our unity and diversity. Make it Happen: We navigate challenges with tenacity, resilience, and a forward-thinking mindset, always holding ourselves accountable for delivering impactful results. As a Key Account Manager (KAM), Thüringen, you will play a critical role in establishing Cytokinetics’ commercial presence in Germany and launching its first product, a novel cardiac myosin inhibitor for Hypertrophic Cardiomyopathy (HCM). This is a unique opportunity to be part of a first-wave commercial build-out, where you will be accountable for developing relationships with leading hospitals, cardiology centers, and specialty networks across your territory. The KAM will act as a trusted partner to healthcare professionals (HCPs), institutions, and patient access stakeholders while working cross-functionally with medical, market access, and patient support colleagues. Success in this role requires a strong combination of strategic account management, clinical acumen, and entrepreneurial drive to ensure that patients with HCM have timely access to innovative therapies. Responsibilities Deliver sales results, work autonomously, and serve as single point of accountability for the successful launch within your territory Develop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues Be a subject matter expert and resource to customers through the delivery of clinically relevant disease and product information while focusing on creating demand for the product launch Communicate approved resources to HCPs for the benefit of HCM patients such as marketing materials, payer information, formulary coverage, patient support services, and educational programs &nbsp;Qualifications Bachelor's Degree is required 5+ years of experience in biotech/pharma sales required Experience as a rep with sole ownership of the territory is highly preferred Cardiology, rare disease, or specialty product experience is preferred Specialty product launch experience is preferred Experience with patient service hubs and specialty pharmacy distribution is preferred Knowledge of KOLs and key accounts within assigned territory is preferred Expertise in evaluation of territory market trends and strategic planning that drives results and exceeds sales objectives is required Experience selling to complex accounts, identifying influential stakeholders, and meeting patient needs is required Clinical acumen with a passion for understanding and championing the needs of customers and their patients, required Agree to credentialing requirements for access to academic institutions, medical facilities, and organizations that are in the assigned territory is required Willing and able to travel overnight, 25% to 75% depending on business needs and geography is required Ability to demonstrate an acceptable driving record and valid driver’s license to operate a company vehicle Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Key Account Manager Thüringen

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.As part of the Commercial organization, this role plays a key role in driving the marketing strategy and execution for innovative cardiovascular therapies across France &amp; Benelux. Reporting to the Head of Commercial France &amp; Benelux, the position combines strategic contribution with strong operational leadership to support successful product launches and sustainable brand growth. The role works in close partnership with cross-functional teams including Medical Affairs, Regulatory, Market Access, and Sales, as well as with Global and Regional Marketing counterparts. The incumbent contributes to the adaptation and evolution of brand strategy, ensures effective omnichannel execution, and supports business performance while maintaining full compliance with internal and external requirements. Key Responsibilities Lead the development, adaptation, and delivery of local marketing strategies and plans in alignment with global and regional brand frameworks. Contribute to the evolution of brand positioning, value propositions, and lifecycle priorities by integrating local market insights, competitive intelligence, and customer needs. Build and steer comprehensive pre-launch, launch and post-launch plans, ensuring cross-functional alignment, planning and execution readiness. Translate scientific and clinical data into clear, compelling, and differentiated customer narratives. Drive omnichannel engagement initiatives to effectively engage healthcare professionals through digital platforms, congresses, and face-to-face interactions. Partner with Sales leadership to support field force enablement, including training on brand strategy, campaigns, and tools. Lead market research activities and competitive analysis to inform both tactical decisions and forward-looking planning. Act as a key partner to Medical Affairs, Regulatory, Market Access, and Sales teams to ensure integrated, compliant brand execution. Serve as a primary interface with Global and Regional Marketing teams, providing local market input and contributing to broader strategic discussions. Manage relationships with external agencies, media partners, and event organizers to ensure high-quality delivery aligned with brand objectives. Plan and oversee the company’s participation in national and regional congresses, symposia, and educational initiatives. Own and manage marketing budgets and financial processes in line with strategic and operational priorities. Monitor brand performance, launch progress, and key business risks, providing regular updates to local and EU stakeholders. Ensure compliance with company SOPs, promotional codes, and applicable regulations, while supporting continuous improvement of marketing processes and ways of working. Provide leadership and direction to marketing resources and extended cross-functional contributors to drive accountability and performance. Contribute to the definition of operational priorities and resourcing to support business objectives. Support the development of marketing capabilities, best practices, and cross-functional collaboration within the affiliate. Qualifications &amp; Experience Bachelor’s degree in science, pharmacy, or medical science; an advanced degree in marketing, business administration, or a related field is preferred. Significant experience in pharmaceutical marketing, omnichannel strategy, or related commercial roles, including leadership of country-level launches. Experience in cardiovascular and/or specialty products, ideally within competitive or innovative therapeutic areas. Strong scientific acumen with the ability to translate complex clinical data into impactful marketing strategies. Solid understanding of laws, regulations, and codes governing communication with healthcare professionals. Demonstrated project management experience with strong planning, prioritization, and cross-functional coordination skills. Experience working with external agencies and partners (digital, media, events, congresses). Excellent interpersonal, communication, and presentation skills. Fluency in French and English. Key Competencies Strategic and analytical thinking combined with a hands-on, execution-oriented approach. Strong leadership presence with the ability to influence and collaborate across functions and levels. Ability to operate effectively in complex and evolving environments. High level of organizational rigor and ability to manage multiple priorities. Clear and concise communication skills, with the ability to convey complex information effectively.#LI-ONSITE Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Marketing Director France & Benelux

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Cytokinetics is a growing biotech company and is looking for a hands-on, highly adaptable Office &amp; Operations Manager to support the daily operations of its France &amp; Benelux affiliate. Reporting directly to the General Manager France &amp; Benelux, this is a fully operational, all-rounder role in a lean, fast-moving biotech environment. The position combines executive assistance, office management, and operational coordination, with a strong focus on getting things done efficiently and pragmatically. The successful candidate will be comfortable wearing multiple hats, managing ambiguity, and stepping in wherever needed to keep the affiliate running smoothly. This role is ideal for someone who is resourceful, proactive, quick, and not afraid of hands-on execution, from high-level coordination to day-to-day practical tasks. Key Responsibilities Provide day-to-day administrative and organizational support to the France &amp; Benelux affiliate. Manage calendars, coordinate meetings, prepare materials, and ensure follow-up on actions. Support planning and logistics for leadership meetings and internal touchpoints. Take full ownership of the day-to-day functioning of the affiliate, ensuring teams have what they need to operate efficiently. Manage office-related topics end-to-end, including: office setup and organization equipment, supplies, and workplace needs coordination with IT and local service providers Support a flexible, hybrid working environment for office-based, remote, and field teams. Act as the go-to person for practical, operational questions from affiliate employees. Coordinate onboarding for new hires (workspace, IT equipment, access, practical setup). Handle a wide range of operational and administrative tasks with a pragmatic, solution-oriented mindset. Provide hands-on operational support and coordination for affiliate activities across commercial and medical teams Coordinate logistics for meetings and external events involving healthcare professionals (HCPs), such as congresses, symposia, advisory boards, and educational meetings. Act as an operational interface between internal teams and external vendors to ensure smooth execution. Independently manage and follow up on operational requests, ensuring timelines are met and issues are resolved quickly. Coordinate the initiation, tracking, and administration of contracts with external vendors, including: event and logistics providers service vendors speakers and HCP engagements Work closely with Legal, Procurement, and Finance to support contract review, approval, and execution. Manage purchase orders, invoice tracking, and vendor onboarding in a lean and efficient way. Maintain clear, structured, and audit-ready documentation of contracts and vendor files. Support tracking of operational and event-related expenses against approved budgets. Maintain simple, efficient filing systems for affiliate documentation (contracts, financial records, compliance documents). Ensure operational activities are executed in line with internal SOPs and compliance requirements, using a practical and pragmatic approach. Support the roll-out and documentation of internal processes and SOPs as the organization evolves. Required Qualifications &amp; Experience Bachelor’s degree or equivalent professional experience. 4–6+ years of experience in a similar hands-on role (Executive Assistant, Office Manager, Operations Coordinator), ideally within biotech, pharmaceutical, or healthcare environments. Experience supporting senior leadership in small, growing, or matrix organizations. Comfortable working in a fast-paced, sometimes ambiguous environment where priorities can shift. Proven experience with vendor coordination, contracting support, and administrative financial processes. Strong organizational skills with a pragmatic, execution-focused mindset. High level of attention to detail, reliability, and follow-through. Excellent interpersonal and communication skills. Fluency in English and French Strong proficiency with standard office tools and administrative systems. Hands-on, resourceful, and solution-oriented. Comfortable doing a bit of everything and switching priorities quickly. Proactive self-starter who takes ownership and gets things done. Calm, reliable, and efficient under pressure. Trusted operational partner for leadership and teams. Flexible, pragmatic, and comfortable in a biotech “build-as-you-go” environment.#LI-ONSITE Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Office & Operations Manager France Benelux

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. Reporting to the VP, General Manager UKIN, the Commercial Director will lead all commercial activities in the region, including sales, marketing, and stakeholder engagement. They will drive launch readiness for aficamten, build strong relationships with healthcare professionals, payers, and regulators, and shape Cytokinetics’ commercial strategy across the countries of responsibility. The role requires both strategic and operational leadership with deep UK healthcare knowledge, proven success in specialty product launches, and the ability to thrive in a fast-paced, entrepreneurial environment. As the company grows, the role will expand to include future product launches and broader commercial initiatives. As a senior leader, the role requires deep expertise in UK and (ideally) Nordic/Irish healthcare systems, a proven track record in launching specialty therapies, and the ability to lead complex, multidimensional programs with significant corporate impact. The successful candidate will operate with a 1–3 year planning horizon, translating global strategy into regional execution, and influencing decisions that affect the long-term success of the UKIN organisation. Key responsibilities: Strategic Leadership and cross-functional collaboration Develop and execute the UKIN commercial strategy for Cytokinetics assets. Implement UKIN commercial plans aligned with global and European objectives. Represent the commercial function on the UKIN Senior Leadership team. Monitor market dynamics and competitor activity to inform strategic decisions. Foster a culture of innovation, accountability, and patient-centricity, aligned to the Cytokinetics values. Work collaboratively across other functions to ensure customer needs are met. Sales team leadership Lead and manage the customer-facing field team to achieve regional sales targets. Recruit, develop, manage and retain a high-performing customer-facing commercial team. Establish performance standards, CRM systems KPIs and incentive schemes, driving a high performance culture by implementing minimum standards. Drive a high-performance culture through coaching, development, and operational excellence. Collaborate with market access to ensure alignment with payer and provider needs. External Cytokinetics ambassador with key centres/customers, supporting commercial uptake. Marketing Leadership Build and lead the UKIN marketing team, ensuring strategic alignment with global brand plans. Oversee development and execution of campaigns, congress strategies, and educational initiatives. Ensure compliance with regulatory standards and internal SOPs. Manage external vendors and agencies to deliver high-impact programs. Financial &amp; Operational Oversight, business planning Own the UKIN sales and marketing P&amp;L, delivering on revenue and profitability targets. Ensure operational excellence and compliance across all commercial activities. Lead the sales and marketing annual business planning process Set territory level budgets and forecasts aligned to country level aspirations Qualifications and experience Bachelor's degree in Life Sciences, Business, or related field; MBA or advanced degree preferred. 10+ years of commercial experience in the UK pharmaceutical or biotech industry, with proven success in launching and commercialising specialty or innovative therapies. Strong understanding of UK healthcare systems, market access pathways, and regulatory frameworks. Exceptional leadership, communication, and stakeholder management skills. ABPI certified Ideally experience in cardiology or rare diseases Entrepreneurial mindset with the ability to thrive in a fast-paced, evolving environment. Strong analytical and strategic thinking capabilities. Proven ability to lead, inspire, and drive high-performing teams, with experience in matrixed and cross-functional collaboration Ideally experience in a small company environment #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Commercial Director

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. Reporting to the Senior Medical Director for the UK, Ireland and Nordics the Senior Medical Science Liaison / Medical Science Liaison (Snr MSL / MSL) is a scientific professional who serves as a key field-based scientific resource for healthcare providers, patients, industry partners and internal colleagues. This role will come with high visibility in our company including critical cross-functional relationships across Medical Affairs, Clinical Development / Operations, and Commercial.&nbsp; This role will focus on key opinion leaders and other HCP’s in the hypertrophic cardiomyopathy therapeutic area, but also support pipeline products in development. Our passion is anchored in rigorous and diligent scientific and clinical approaches to the discovery and development of novel mechanism therapeutics. With gratitude for the commitments and convictions of our employees who are inspired by the courage of patients we aim to serve, we believe Cytokinetics will continue to be a pioneering, values-driven, sustainable, fully integrated biopharmaceutical company. &nbsp; Baseline MSL Responsibilities: Identify national, regional, and local Key Opinion Leaders (KOLs) involved in the provision of cardiovascular care within institutional care centres and engage them in proactive and reactive scientific exchange Maintain and broaden professional relationships with HCPs (Physicians, Specialist Nurses, Echocardiologists, Genetic Counsellors, Pharmacists (and other relevant members of the multi-disciplinary team) in institutional care centers, to expand research, advisory, and educational partnership opportunities; identify areas of unmet medical need; and assure thoughtful exchange of current medical information related to products in development and therapeutic areas of importance Serve as a scientific expert at key medical and scientific conferences, advisory boards, clinical investigator meetings, internal meetings, and patient advocacy group meetings Maintain a high-level of scientific knowledge and understanding about disease state, underlying science, treatment guidelines, available treatment agents and options, as well as other relevant therapies under development Maintain a superior understanding of current trends in clinical research, competitive developments, patient care, and their impact on Cytokinetics’ medical strategies Work with Medical Affairs and other internal colleagues on initiatives including medical information, publications, medical education, grants, speaker training, and other educational programs Provide support to our clinical development programs by serving as a key point of contact for company-sponsored trial investigators, investigator-initiated research, and registries consistent with company objectives and regulations Generate Field Medical Affairs plans to identify collaborative opportunities with KOL’s and institutions, review scientific program of relevant conferences, attend sessions, support exhibit booth operations, and contribute to a timely written conference report summarizing key information, activities, and competitive intelligence to colleagues Accurate and timely documentation of activities within applicable company databases and platforms In addition to above, for Senior Medical Science Liaison: Mentor, train and support other Medical Scientists Provide scientific training on key relevant data to Key Account Managers and other business colleagues as required Provide strategic input and execute region-specific plans to achieve KOL engagement goals and Medical Affairs departmental goals Pursue projects independently with a high degree of quality and timely execution Contribute to / lead Congress Planning activities Maintain a complete awareness of and understanding about current “real world” clinical practices, HEOR drivers, and emerging trends in treatments/medicine Establish relationships with key executive leadership colleagues across Cytokinetics and connect external parties with appropriate leadership team members Qualifications Advanced clinical or scientific degree (BSc, MSc, BPharm, MPharm, PhD, BM BS or equivalent) preferred Minimum of 2-5 years of MSL experience for Snr. MSL. &nbsp;Experience in cardiovascular therapy area and / or hypertrophic cardiomyopathy is preferable. Experience in heart failure is beneficial but not required. Final position level will be determined based on overall experience Must be analytical and articulate in both oral and written communications, possess excellent presentation skills, with a demonstrated ability to communicate well with external stakeholders and all internal levels of the organization Must possess knowledge of the Medical Science Liaison roles and responsibilities and understand compliance within the ABPI Code Standards for Interactions with UK Healthcare Providers and all other company policies, rules and regulations Comply with all credentialing requirements for any healthcare institution which is part of the Medical Science plan, including, among other things, routine background checks, medical testing or proof of immunisations, training on facility policies, and adherence to confidentiality and/or other agreements Proficiency with Microsoft Office and web-based applications A valid Driver’s License and good driving record are required Ability to travel both domestically (~30%-50%) and internationally on occasion (TBD) #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Senior Medical Science Liaison / Medical Science Liaison

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. The Associate Legal Counsel, Europe will be responsible for providing legal support (including, legal advice, &nbsp;drafting, review, and negotiation of a wide range of commercial agreements) for our Cytokinetics European affiliates. This position will act as a business partner to the Commercial, Medical Affairs, Market Access, Procurement, and other cross-functional teams supporting our operations Europe (primarily in Switzerland, the UK, Ireland, Spain, Italy, France, and Germany) and will support senior counsel on complex matters This role requires a diverse skill set across contracts, legal operations, and general legal counseling. The role is based at the Company Regional Headquarter in Zug, Switzerland, and reports to the Head of Legal and Compliance, Europe. Key Responsibilities Contract Drafting, Negotiation &amp; Management Draft, review, and negotiate a variety of contractual agreements, including: Non-Disclosure Agreements (NDAs) Master Services Agreements (MSAs) and associated Statement of Work (SOWs) HCP/HCOs agreements Vendor/supplier agreements Event and meeting agreements Distribution/Wholesaler agreements Data protection–related contract terms (in collaboration with Privacy Counsel) Ensure contract terms are aligned with Cytokinetics’ legal, compliance, and operational standards and company policies. Collaborate with business partners to understand objectives and craft practical, risk-appropriate solutions. Legal Support &amp; Cross-Functional Collaboration Provide day-to-day legal support to EU business functions and resolve issues as they arise. Advise teams on a range of legal issues and contract processes, company policies, and best practices to manage risks and improve efficiency and compliance. Work closely with the US-based legal team to ensure consistency in approach and support and contribute to legal projects and initiatives as required. Legal Operations Assist with developing and maintaining&nbsp; contract templates, playbooks, and clause libraries for Europe. Provide input and support to US-based team to tailor our Contract Lifecycle Management (CLM) system to European needs, roll out the implementation and its ongoing management thereafter. Help identify opportunities to streamline contracting workflows and improve operational efficiency. Compliance &amp; Risk Management Identify and provide advice on a range of legal risks appropriately, ensuring our operations comply with applicable EU and country-specific requirements. Partner with Head of Legal and Compliance, Compliance Officer, Regulatory, Finance &nbsp;and Procurement teams when contract matters intersect with finance, regulatory or compliance considerations. Qualifications Juris Doctor (JD) degree or other advanced law degree. Bar qualification in Switzerland or another European jurisdiction, desirable. Approximately 7+ years of experience, in life sciences, healthcare, or related industries with a strong preference for candidates who have experience in the biotech or pharmaceutical industry with direct experience across multiple European jurisdictions. Demonstrated ability to proactively identify, analyze, and manage complex legal issues and provide strategic, proactive legal advice and business-oriented solutions. Experience working with Privacy and Data Protection matters and deep understanding of the current legislation is highly desirable Strong negotiation, drafting, and legal analytical skills with the ability to balance legal risk with practical business needs. Solid judgment and business acumen and understanding of business operations, particularly in determining the significance of legal matters in the context of business objectives, assessing risks and benefits and providing innovative business and legal solutions. Experience working with Contract Lifecycle Management (CLM) systems. Excellent written and verbal communication skills; fluency in English required, additional fluency in at least another European language is highly valued. Enthusiastic, self-motivated and efficient, able to proactively identify short and mid-term business needs, to develop strategies and to manage responsibilities independently as well as to facilitate teamwork and to mentor and guide peers. Strong organizational skills in order to prioritize and manage multiple time-sensitive projects simultaneously; Able to work accurately with an appropriate sense of urgency and function effectively and efficiently in a fast-paced and dynamic environment Strong interpersonal skills, including diplomacy and flexibility, and the ability to interface effectively throughout all levels of the organization as well as with external parties, and adaptable to circumstances and variety of cultures. Hands-on, collaborative mindset with a willingness to take on a broad range of responsibilities. #LI-HYBRID &nbsp; &nbsp; &nbsp; &nbsp;Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Associate Legal Counsel, Europe

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. The Compliance Director, Europe will partner with our Head of Legal &amp; Compliance, Europe to lead compliance support for our European organisation (including Switzerland, Germany, the UK, Ireland, Spain, Italy, France). This individual will be responsible for helping to design, implement, and operationalize a robust European ethics and compliance program in alignment with global standards and local regulatory expectations. The role is based at the company European headquarter in Zug, Switzerland, and reports to the Head of Legal and Compliance, Europe. The ideal candidate is a proactive, solutions-oriented compliance professional who can operate strategically with senior leadership while rolling up their sleeves to support day-to-day compliance needs. This leader will partner closely with the European leadership team and key stakeholders (Commercial, Medical Affairs, Regulatory, HR, and Legal teams) to foster a culture of integrity and ethical conduct in the region. Key Responsibilities Strategic Leadership &amp; Compliance Program Development Develop and refine Cytokinetics’ European compliance strategy, aligned with European compliance frameworks and emerging regulatory trends. Establish policies, procedures, and processes across the region to ensure compliance with country-specific regulations. Serve as a Compliance business partner to regional leadership teams, helping anticipate risks and implement proactive mitigation strategies. Act as a trusted advisor to key stakeholders in the region including Commercial and Medical teams to help build their strategies as we prepare for&nbsp; product launches. Operational Compliance &amp; Hands-On Execution Lead key operational compliance activities, including review and approval of promotional and non-promotional materials, training delivery, monitoring, risk assessments, investigations, and transparency reporting. Manage local compliance operations in each region, ensuring consistency while accounting for country-specific requirements. Oversee process implementation for third-party due diligence, audits, and vendor compliance. Governance, Training &amp; Culture Building Design and deliver engaging compliance training across functions and countries. Provide practical guidance, on relevant Compliance topics including ABAC, Privacy and internal policies, transparency, and evolving regulatory expectations. Promote a strong culture of ethics and accountability, serving as a visible compliance champion throughout Europe. Drive continuous improvement in compliance systems, monitoring programs, and reporting structures. Support global compliance governance forums and contribute to enterprise-wide compliance strategy. Support investigations into potential compliance violations and work with Legal and HR on remediation and corrective action Qualifications Bachelor’s degree required, advanced degree in Law, Life Sciences, Business, or related field preferred.10+ years of relevant European Compliance experience within the biopharma industry supporting Commercial and Medical Affairs teams. Law degree is plus. Strong knowledge of European and major country-level compliance frameworks and codes, including EFPIA, Loi Bertrand, ABPI and other local relevant anti-bribery/anti-corruption regulations, GDPR and other privacy regulation and guidance. Experience working in a fast-paced, evolving environment; launch experience strongly preferred. Track record of building compliance programs that balance risk mitigation with business enablement. Demonstrated ability to work at both strategic and operational levels. Excellent judgment, communication, and stakeholder management skills. Ability to operate independently and influence without authority in a matrixed global organization. Ethics &amp; Compliance certification (CCEP, CPA, CIA, etc.) and Privacy certification are a plus. Fluent in English; additional European languages (German, French, Spanish) are highly desirable. Strong interpersonal skills, including diplomacy and flexibility, and the ability to interface effectively throughout all levels of the organization as well as with external parties, and adaptable to circumstances and variety of cultures. Travel (20%) #LI-HYBRID &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Compliance Director, Europe

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. Reporting to the VP, General Manager France &amp; Benelux, the Head of Commercial is responsible for leading all commercial activities across France and Benelux, including sales, marketing, and stakeholder engagement. This role combines strategic vision with operational excellence to successfully launch, establish, and grow our products in these markets, ensuring alignment with regional and global priorities and achieving national and regional targets. As a key member of the Country Leadership Team, the Head of Commercial will inspire and develop a high-performing team, engage with external stakeholders to expand patient access, and collaborate closely with EU &amp; global teams. Acting as an enterprise leader, the incumbent will demonstrate patient focus, an owner mindset, and foster collaboration to drive impact. Key ResponsibilitiesStrategic Leadership &amp; Cross-Functional Collaboration Define and execute the commercial strategy for France &amp; Benelux, aligned with global and European objectives. Represent the commercial function on the Country Leadership Team. Collaborate actively with Global, EU &amp; local teams to share insights, benchmark performance, and implement best practices. Monitor market dynamics and competitor activity to inform strategic decisions. Develop and implement market research initiatives to inform strategy, track performance, and guide decision-making. Foster a culture of innovation, accountability, and patient-centricity. Ensure all commercial activities comply with the company’s Code of Conduct and local pharmaceutical regulations. Sales &amp; Marketing Leadership Lead and manage the sales and marketing teams to achieve national and regional targets. Recruit, develop, manage, and retain a high-performing commercial organization (Sales Managers, Key Account Managers, Marketing). Establish performance standards, CRM systems, KPIs, and incentive schemes. Drive a high-performance culture through coaching, development, and operational excellence. Oversee development and execution of integrated marketing campaigns, congress strategies, and educational initiatives. Manage external vendors and agencies to deliver high-impact programs. Ensure compliance with regulatory standards and internal SOPs. Financial &amp; Operational Oversight Own the France &amp; Benelux commercial P&amp;L, delivering on revenue and profitability targets. Manage budgets and resources effectively, ensuring alignment with launch and growth objectives. Track and analyze performance against forecasts and KPIs, adjusting strategy as needed. External Engagement Act as company ambassador with key stakeholders (healthcare professionals, payers, regulators). Engage directly with external stakeholders through customer-facing activities (joint visits, KOL meetings, congresses, and events). Profile &amp; Qualifications Extensive experience in pharmaceutical commercial leadership in France; knowledge of Benelux healthcare systems is a plus. Fluent in English Minimum 10 years’ experience in pharmaceutical sales, marketing, or commercial leadership roles. Ideally experience in cardiology or rare diseases. Strong analytical and strategic thinking capabilities. Proven ability to lead, inspire, and drive high-performing teams, with experience in matrixed and cross-functional collaboration. Ideally experience in a small company environment. University degree in Life Sciences, Business, or related field (Master’s or MBA preferred). #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Head of Commercial France & Benelux

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.It’s an exciting time to join Cytokinetics. We’re seeking trailblazing, results-oriented sales and marketing professionals who are ready to embrace this exciting opportunity to make a significant impact and shape the future of our company. As part of the Commercial organisation, the Marketing Lead, UK, Ireland and Nordics plays a key role in driving the marketing strategy and execution for innovative cardiovascular therapies across the UK, Ireland and Nordics (UKIN). Reporting to the Head of Commercial (UKIN), the position combines strategic contribution with strong operational leadership to support successful product launches and sustainable brand growth. The role works in close partnership with cross-functional teams including Medical Affairs, Regulatory, Market Access, and Sales, as well as with Global and Regional Marketing counterparts. The incumbent contributes to the adaptation and evolution of brand strategy, ensures effective omnichannel execution, and supports business performance while maintaining full compliance with internal and external requirements. Key Responsibilities Lead the development, adaptation, and delivery of local marketing strategies and plans in alignment with global and regional brand frameworks. Contribute to the evolution of brand positioning, value propositions, and lifecycle priorities by integrating local market insights, competitive intelligence, and customer needs. Build and steer comprehensive pre-launch, launch and post-launch plans, ensuring cross-functional alignment, planning and execution readiness. Translate scientific and clinical data into clear, compelling, and differentiated customer narratives. Drive omnichannel engagement initiatives to effectively engage healthcare professionals through digital platforms, congresses, and face-to-face interactions. Partner with sales leadership to support field force enablement, including training on brand strategy, campaigns, and tools. Lead market research activities and competitive analysis to inform both tactical decisions and forward-looking planning. Act as a key partner to the Medical Affairs, Regulatory, Market Access, and Sales teams to ensure integrated, compliant brand execution. Serve as a primary interface with Global and Regional Marketing teams, providing local market input and contributing to broader strategic discussions. Manage relationships with external agencies, media partners, and event organisers to ensure high-quality delivery aligned with brand objectives. Plan and oversee the company’s participation in national and regional congresses, symposia, and educational initiatives. Own and manage marketing budgets and financial processes in line with strategic and operational priorities. Monitor brand performance, launch progress, and key business risks, providing regular updates to local, EU and global stakeholders. Ensure compliance with company SOPs, promotional codes, and applicable regulations, while supporting continuous improvement of marketing processes and ways of working. Provide leadership and direction to marketing resources and extended cross-functional contributors to drive accountability and performance. Contribute to the definition of operational priorities and resourcing to support business objectives. Support the development of marketing capabilities, best practices, and cross-functional collaboration within the affiliate. Qualifications &amp; Experience Bachelor’s degree in science, pharmacy, or medical science; an advanced degree in marketing, business administration, or a related field is preferred. Demonstrated successful marketing leadership of speciality launches, including full-omnichannel approach. Significant experience (5+ years) in pharmaceutical marketing, omnichannel strategy, or related commercial roles. Experience in cardiovascular and/or specialty products, ideally within competitive or innovative therapeutic areas. Strong scientific acumen with the ability to translate complex clinical data into impactful marketing strategies. Solid understanding of ABPI regulations. Demonstrated project management experience with strong planning, prioritisation, and cross-functional coordination skills. Extensive experience working with vendor management/external agencies and partners (digital, media, events, congresses). Excellent interpersonal, communication, and presentation skills. Key Competencies Strategic and analytical thinking combined with a hands-on, execution-oriented approach. Strong leadership presence with the ability to influence and collaborate across functions and levels. Ability to operate effectively in complex and evolving environments. High degree of autonomy, with a can-do, self-starting attitude. High level of organisational rigour and ability to manage multiple priorities. Clear and concise communication skills, with the ability to convey complex information effectively. #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Marketing Lead (Senior Product Manager) UK, Ireland, and Nordics

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. About the Role:&nbsp;We are seeking an experienced Market Research Manager to support strategic decision-making through innovative research approaches. This role will lead primary market research initiatives across the major EU Markets, evaluate brand performance, and provide critical insights to support our commercial growth and product launches in Europe. This position reports directly to the&nbsp;Head of Analytics Europe Key Responsibilities: Manage primary and secondary market research projects from inception to completion, including vendor selection, questionnaire development, data analysis, and strategic recommendations Support the implementation of innovative market research methodologies and solutions Provide SME guidance on study design, research materials, and optimization opportunities across multiple concurrent projects Collaborate with cross-functional teams to develop data-driven strategies supporting product launches, marketing campaigns, and sales initiatives Provide insights and recommendations to senior leadership aligned with brand objectives and country-specific needs. Collaborate with US market research teams to optimize study materials, share insights, and implement best practices Support forecasting teams with validated market research inputs and assumptions Develop comprehensive understanding of disease states, competitive landscape, and market dynamics across major EU markets Monitor and evaluate brand performance, market trends, and marketing initiative effectiveness Track commercial launch preparation and performance, providing strategic commentary to senior management Manage market research budget and vendor relationships with focus on cost optimization and quality delivery Ensure compliance with pharmacovigilance requirements and regulatory standards Support continuous improvement initiatives in data analysis methodologies Experience &amp; Background Bachelor's / Master’s degree in business in Statistics/Mathematics, Medicine, Sciences, Health Economics, Sociology, or Psychology 10+ years&nbsp;of market research experience within pharmaceutical companies or specialist agencies Experience collaborating with European markets and multicultural teams Strong understanding of pharmaceutical sales, marketing processes, and disease areas Core Competencies Exceptional communication and presentation skills with ability to influence at all organizational levels Strong analytical mindset with ability to identify actionable insights and strategic recommendations Excellent project management capabilities including scoping, defining deliverables, and senior-level reporting Proven ability to thrive in fast-paced environments with strong sense of accountability Discretion and ability to handle sensitive and confidential information Solution-oriented approach with strong business acumen Advanced proficiency in Microsoft Office suite, particularly Excel Working knowledge of statistical analytical techniques is nice to have #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Market Research Manager

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. Cytokinetics is seeking an experienced Senior Recruiter to join our Global Talent Acquisition team on a long-term contract at our European office in Zug, Switzerland. The ideal candidate will bring a deep knowledge of recruiting practices across Europe, and will thrive in a dynamic, fast-paced growing environment. You’ll partner closely with regional and country business leaders, HR stakeholders, and external agencies to attract critical talent that aligns with Cytokinetics’ mission, core values, and culture. Key Responsibilities Lead full-cycle recruitment for a variety of roles across European countries, including sourcing, screening, interviewing, and managing the offer process. Proven track record managing the end-to-end process—intake, sourcing, screening, interviewing, offer negotiation, and onboarding. Experience with both commercial (sales/marketing) and scientific/medical (MSL, regulatory) profiles Develop and execute tailored sourcing strategies to attract talent in markets to build and enhance Cytokinetics’ brand. Sourcing and market mapping: Skilled at building pipelines for hard-to-fill roles using LinkedIn Recruiter, Boolean search, and targeted outreach. Experience conducting competitive market intelligence on talent availability and compensation across European countries. Stakeholder management. Partner with European business leaders and HR leader to understand business and hiring needs and develop tailored recruitment strategies. Manage external recruiting agencies, especially high-volume hiring (e.g., sales teams), ensuring alignment with hiring goals and budget. Help shape and implement EU-specific recruiting processes and workflows, balancing global standards with local nuances. Manage and optimize recruitment processes within our Applicant Tracking System, Workday Recruiting. Support the transition from Greenhouse to Workday Recruiting, contributing to system setup and optimization. Build and maintain pipelines of qualified candidates for current and future openings. Collaborate closely with the broader TA and HR team to ensure a consistent, high-quality candidate and hiring manager experience. Provide market insights and recruitment analytics to help guide data-driven decisions. Ensure compliance with local labor laws, internal policies, and any evolving employment needs across the countries supported Qualifications &amp; Experience Minimum 7 years of full-cycle recruitment experience within a global organization, ideally in the pharmaceutical, biotechnology, or life sciences industry. Demonstrated experience recruiting across multiple European markets, with a deep understanding of local hiring practices, regulations, and cultural nuances. Familiarity with local recruiting practices, labor laws, and candidate expectations in key markets (UK, Germany, France, Spain, Italy). Ability to manage multi-country recruitment with attention to language and cultural nuances. Experience managing and collaborating with external recruiting partners and volume hiring campaigns. Hands-on experience using Workday Recruiting or similar applicant tracking systems. Strong communication and stakeholder management skills with the ability to influence, be agile and flexible, and advise hiring leaders. Project management skills with the ability to lead, collaborate, and partner with our HR colleagues across various teams Familiarity working in a fast-paced, matrixed, and evolving environment. Fluent in English; proficiency in other European languages (such as German, French, Spanish, or Italian) is a plus. Comfortable working in a fast-paced, matrixed environment with limited infrastructure. Based in or near Zug, Switzerland, with ability to work onsite or in a hybrid capacity. Preferred Qualifications Experience supporting a commercial launch and expansion in Europe. Knowledge of employer branding and sourcing best practices across diverse European markets Project management skills and ability to build and execute scalable recruiting processes. &nbsp; #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Contract Senior Recruiter, Europe

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.As Associate Director, Sourcing &amp; Supplier Relationship Management, you will play a critical role in ensuring the suppliers and partners we work with meet our high standards for quality, innovation, and patient impact. This role plays a critical part in the comprehensive lifecycle of Cytokinetics relations with partners and suppliers supporting Global Supply Chain &amp; Technical Operations. This role requires strong strategic thinking, broad industry experience and excellent relationship development and management skills. This role will support our Sourcing and Network Strategy pillar, a key component of our Global Supply Chain &amp; Technical Operations strategy.&nbsp; This role will support our Manufacturing and Lab Services Supplier Strategy, marketplace assessments of supplier capabilities from early development thru post approval Commercialization, supplier due diligence through Request for Information (RFI) and Requests for Proposals (RPF). These due diligence activities will lead to collaborative supplier selection, contract negotiations, operationalization of the relationship and ultimately management of supplier performance against the contract. This role will be a key partner to CMC and Technical Operations, External Manufacturing and Supply Operations, Enterprise Risk Management, Supply Planning and Partner Pillar activities, and the Supply Chain Center of Excellence in Dublin Ireland. This role requires demonstrated business acumen, influencing skills, strategic thinking, relationship building and collaboration behaviors. Responsibilities Strategic Supplier Management Develop and execute sourcing and network strategies that align with Global Supply Chain &amp; Technical Operations goals. Serve as the primary commercial point of contact for assigned CMOs, Labs and critical suppliers. Conduct marketplace assessments, supplier segmentation, and due diligence (RFIs/RFPs). Collaborate with Enterprise Risk Management to identify and mitigate supplier sourcing risks. Contracting &amp; Negotiations Lead supplier selection, contract negotiations, and agreement development in partnership with Legal, Finance, Procurement, and Quality. Support External Supply team with contract setup, budget planning, and tracking. Performance &amp; Risk Management Monitor supplier performance using standard KPIs and ensure compliance with contractual and regulatory requirements. Support supplier audits and develop business continuity and risk management processes. Identify opportunities to improve supplier value, cost, quality, and service. Collaboration &amp; Leadership Partner with CMC, Technical Operations, Supply Planning, and global teams in Dublin, Ireland. Represent Supply Chain Sourcing on cross-functional teams for complex projects. Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Qualifications Bachelor’s degree in Biology, Chemistry, Engineering, or related field (advanced degree a plus). 10+ years of experience in Life Sciences, Engineering, Business, or Supply Chain, preferably within Biotech/Pharma. Strong understanding of product development, GMP manufacturing, and related regulations (cGMP, GCP, CFRs, Part 11, FDA/EMA Guidelines). Proven expertise in manufacturing cost benchmarks and pricing strategies for small molecule manufacturing. Demonstrated success in supplier relationship management, contract negotiation, and strategic sourcing. Strong communication, collaboration, and influencing skills. ERP systems experience, preferably Oracle Ability to travel domestically and internationally (15–20%). #LI-HYBRIDOur passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do –all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves.Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Associate Director, Sourcing & Supplier Relationship Management

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. The Interim Director, HR Business Partner Southern Europe serves as the strategic HR partner for Italy and Iberia, supporting the company’s first EU commercial launch planned for 2026–2027. Reporting to the Head of HR, Europe with dotted line to VP, GM Italy, this role is responsible for shaping and executing the full end-to-end HR agenda for the region, ensuring organizational readiness, leadership capability, and cultural alignment as the business scales. This position operates within a newly evolving European HR operating model and works in close partnership with business leaders, the European HR team, and global HR Centers of Excellence (CoEs) to deliver consistent, high-impact people solutions while addressing local market needs. Please Note: This role is as 1-year temporary assignment Responsibilities Serve as the primary HR partner and steward of the full HR agenda for Southern Europe, ensuring alignment with European and global business objectives. Partner with senior business leaders to drive performance, organizational capability, and commercial launch readiness, providing strategic counsel through periods of growth and change. Act as a trusted advisor to leaders, influencing decision-making and reinforcing the desired leadership culture and ways of working. Co-own and drive talent, organizational effectiveness, and culture-building initiatives aligned with European and global HR strategy. Lead workforce planning, organizational design, role creation, and headcount planning to support near- and long-term business growth. Support succession planning, leadership development, and long-term talent strategies to ensure leadership continuity and bench strength. Own staffing plans and recruiting pipeline quality for the Italy and Iberia regions, partnering closely with Talent Acquisition and HR Centers of Excellence to deliver high-quality hiring outcomes. Participate in hiring decisions for critical and leadership roles, ensuring alignment with capability, culture, and future-state organizational needs. Lead annual performance management processes, including goal setting, performance reviews, calibration, and development planning. Manage salary and bonus cycles in alignment with regional reward frameworks and corporate guidelines. Coach managers on performance planning, career development, and effective leadership behaviors, building leadership capability across the organization. Ensure consistent deployment of HR systems, policies, reward programs, and people processes in alignment with European and corporate standards, while addressing local requirements. Implement and sustain HR initiatives delivered by HR Centers of Excellence, ensuring effective adoption and change management at the local level. Contribute to European and global HR projects and cross-functional initiatives, representing Southern Europe business needs and perspectives. Develop and execute the annual HR Business Plan aligned with European HR priorities and business objectives. Provide support for HR administration management as required, ensuring compliance, efficiency, and a positive employee experience. Qualifications 10+ years of progressive HR Business Partner or HR Generalist experience with increasing scope, complexity, and leadership responsibility. Bachelor’s degree in Human Resources, Business Administration, or a related field; advanced degree (Master’s or MBA) preferred. Biopharmaceutical or pharmaceutical industry experience strongly preferred, ideally within a commercial environment. Proven success as a strategic HR partner in a build-out, scale-up, or first-market commercial launch environment. Demonstrated experience partnering effectively with HR Centers of Excellence in a global, matrixed organization. Deep knowledge of Italian and Spanish labor law,&nbsp; and works council engagement; experience supporting Italy-and Spain based employee populations required. Strong consulting, communication, and influencing skills, with the ability to operate credibly with senior leaders and cross-functional stakeholders. Experience operating across multiple countries and cultures, with sensitivity to regional and local market dynamics. Strong business acumen with the ability to translate business strategy into people and organizational solutions. Demonstrated change leadership capability, including experience leading organizations through growth, transformation, or ambiguity. Experience leveraging HR systems and tools, such as HRIS (e.g., Workday or equivalent), performance management and talent platforms, compensation planning tools, and workforce analytics, to inform decision-making, ensure compliance, and drive scalable people processes. Fluency in Italian and English. Spanish strongly preferred. #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Interim Director, Human Resources Business Partner, Southern Europe

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Reporting directly to the&nbsp;Director Market Access, DACH, the&nbsp;Senior Field Market Access Manager&nbsp;is responsible for developing and executing market access strategies within Berlin and greater area to ensure optimal patient access to therapies. Working closely with the Director Market Access DACH and cross-functional teams (Sales, Marketing, Medical), the role focuses on: Developing and implementing regional Market Access strategy and tactics by identification of regional prescription and remuneration hurdles, engaging with local payers, federations and healthcare stakeholders, addressing access barriers at hospital and office-based account level in cardiology care. The Senior Field Market Access Manager contributes to regional insights and data analysis, tactical solutions to lead successful reimbursement outcomes, strategic input to align local execution with the broader commercial objectives. This role requires strong stakeholder engagement skills, a deep understanding of regional healthcare dynamics, and the ability to operate independently while collaborating proactively across functions. ROLE RESPONSIBILITIES Stakeholder Engagement and Relationship Management Partner with commercial Key Account Managers with face-to-face, personal and individual HCP education on regional reimbursement and budget regulations in order to address questions regarding funding of high-value specialty care medicines in cardiology (including possibility of individual special practice conditions). Build and maintain strong relationships with regional payers, sick funds, SHI physicians’ associations, hospital controllers, retail pharmacists, and other healthcare decision-makers. Drive regional x-functional collaboration with Commercial and Medical to engage with physician associations and other relevant stakeholders to approach prescription hurdles (e.g. documentation sheet, special regional practice condition). Address and discuss imbalance of national special practice condition within the AMNOG with relevant stakeholders and identify mutual solutions (e.g. regional special practice condition). Explore and, if required, execute contracting strategy: Identify strategic opportunities for regional reimbursement- related agreements and contracts for , including negotiation of the contracts. Prepare and present business cases for such regional agreements to the DACH Leadership Team and in case of approval, lead and monitor execution in practice. Engage with drug evaluation committees and payer organizations to facilitate patient access and reduce funding barriers. Represent the company in compliant interactions, offering value-added solutions to support access and reimbursement. Cross-functional Collaboration Visit HCPs together with commercial Key Account Managers, on a regular basis Collaborate closely with Sales, Marketing, Medical and other internal teams to align on access priorities and ensure coordinated execution. Lead cross-functional projects that enhance regional access and create win-win solutions with stakeholders. Provide tools, training, and insights to support field teams in overcoming market access barriers and pricing concerns of HCPs. Data, Insights &amp; Policy Monitoring Monitor and analyze regional healthcare developments, policy changes, and reimbursement trends. Collect and interpret local data to inform strategic planning and tactical execution. Share insights with internal teams to optimize market access approaches and anticipate challenges. Communication &amp; Training Develop and deliver training presentations for sales teams and external stakeholders on relevant health policy, pricing, and reimbursement topics, tailored to specialty cardiology issues. Create and adapt materials that communicate the value of innovative specialty care products in a way that resonates with regional stakeholders. Present complex market access topics in a clear, audience-appropriate format at internal and external events. Project &amp; Event Management Plan, manage, and monitor regional projects, including contracts and agreements with payers, in coordination with the DACH Management Team. Organize and lead access-related events such as expert meetings, roundtables, and commercial meetings in both hospital and outpatient settings. Use both digital and analogue channels to engage with stakeholders and support collaboration. QUALIFICATIONS AND EXPERIENCE Educational Background A bachelor’s degree is required; an advanced university degree is preferred—ideally in natural sciences, healthcare-related fields, economics or business administration. Additional qualifications in health economics, health policy, or market access are considered a strong asset. Industry Experience Minimum of 8 years of professional experience in the pharmaceutical or biopharmaceutical industry, with a focus on market access, health policy, or reimbursement. At least 5 years of hands-on experience in regional market access or related field-based roles, with a proven track record of executing access strategies operatively at the customer level. Healthcare System Expertise In-depth knowledge of the German healthcare system and self-administration structures, including legal frameworks for pricing and reimbursement in both outpatient and inpatient sectors. A resilient network of regional stakeholders within the German healthcare system, particularly with sick funds and payor bodies. Stakeholder Management and Communication Demonstrated success in stakeholder engagement, with the ability to build and maintain influential networks across regional healthcare institutions. Strong communication and presentation skills, with the ability to convey complex healthcare and policy topics in a clear, audience-appropriate and convincing manner. High motivation, goal orientation, and a collaborative yet independent working style. Cross-functional and Digital Competence Experience working in matrixed, fast-paced environments and managing cross-functional projects. Excellent project management skills, with the ability to handle multiple complex initiatives simultaneously and deliver results on time. IT-savvy, with proficiency in modern digital communication tools and MS Office applications Strategic &amp; Analytical Thinking Strong analytical and strategic thinking capabilities, with a passion for translating complex interrelationships into actionable insights. Interest in health policy developments and their impact on market access and reimbursement. Language and Travel Native-level fluency in German and business-fluent English, both written and spoken. Willingness to travel regularly across the assigned region and the broader DACH area, including frequent overnight trips.#LI-REMOTE Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Senior Field Market Access Manager

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Job Purpose Own the end-to-end technical enablement of Oral Solid Dose (OSD) Drug Product supply for Aficamten and future pipeline candidates across an external CMO network. Deliver robust formulation and process technology transfer, scale-up and PPQ readiness, commercial control strategy, and ongoing CPV to ensure reliable, compliant, and cost-effective DP supply. Drive process robustness, investigations, and continuous improvement, and serve as the primary technical interface to Drug Product CMOs. Operate cross-functionally: provide data packages and technical summaries in partnership with Regulatory/CMC, QA&amp;C, and Supply Chain. Lead the technical plan for dual-sourcing (DP sites, critical excipients, and packaging components) and hand over filing, quality, and commercial actions to the owning functions. Responsibilities External Manufacturing / Technical Operations Lead onboarding and technical oversight of Drug Product CMOs (OSD); provide technical input to MSAs, SoWs, and KPIs. Dual-sourcing – technical enablement: Lead the technical plan to qualify an alternate OSD DP site and/or critical excipient/packaging component source—formulation and process transfer, engineering runs, PPQ readiness, comparability strategy, and CPV set-up—in partnership with Regulatory CMC (filings/variations), QA&amp;C (audits/release), and Supply Chain (commercials/capacity). Own DP tech transfer, scale-up, PPQ strategy, and execution for OSD processes (e.g., blending, granulation, compression, coating, and packaging). Define, implement, and maintain the commercial DP control strategy and CPV plan, including in-process controls, release strategy, and stability support. Drive process robustness and continuous improvement at CMOs; lead and coach investigations (deviations, OOS, OOT, complaints) to root cause with sustainable corrective actions. Regulatory CMC (Drug Product) Partner with Regulatory CMC by providing technical data packages, comparability assessments, and PPQ summaries to support site-addition variations, post-approval changes, and lifecycle updates for OSD Drug Product. Regulatory CMC owns dossier authorship, submissions, and Health Authority interactions (queries, approvals). &nbsp;Quality &amp; Compliance (with QA) Partner with QA&amp;C to supply technical inputs for audits, PAI readiness, and closure of technical actions from deviations and CAPAs. QA&amp;C owns Quality Agreements, external audits, product release/CoA, and QMS governance. Supply, Cost &amp; Risk Partner with External Supply / Supply Chain on CMO selection, contracts, campaign planning, packaging strategy, and inventory/safety-stock, providing the technical plan and readiness timelines. External Supply / Supply Chain owns commercial budget, capacity, and the master supply risk register; Tech Ops owns the DP technical risk register and mitigations (process, formulation, component, and site risks). Analytics / Data &amp; Ways of Working Establish dashboards for yield, throughput, Right-First-Time, OTIF, scrap, and CoGs; trend process and CPV data from DP CMOs. Lead cross-functional operating routines and governance with internal stakeholders and external partners. Qualifications MSc/PhD in Pharmaceutical Sciences, Chemical Engineering, Materials Science, or related discipline. 15+ years in small-molecule Oral Solid Dose Drug Product from late-stage development through commercial manufacturing with CMOs. Proven leadership of DP tech transfer, scale-up, PPQ, commercial control strategy, and CPV. Early-career on-plant OSD manufacturing exposure (granulation, compression, coating). Strong GMP and ICH Q8–Q12 working knowledge (Q9/Q10 applied to DP lifecycle management). Demonstrated DP process robustness: CPP/CMA definition across OSD unit operations, dissolution control, specification setting, and excipient/component strategy. Hands-on leadership of investigations and RCA (OOS/OOT, deviations, complaints) and continuous improvement at external DP sites. Comfortable with statistics, DoE, SPC, and CPV data trending for OSD manufacturing and packaging. Regulatory CMC: Generate high-quality technical content and data packages (comparability, PPQ summaries) and support HA queries; Reg CMC owns dossiers and submissions. QA&amp;C: Provide technical inputs to audits, PAI readiness, and CAPAs; QA&amp;C owns Quality Agreements, release, and QMS. External Supply / Supply Chain: Provide technical plans and readiness dates; they own commercials, capacity, and the master supply risk register. Strong experience in OSD CMO governance, performance management, KPIs, and second-source DP site or component technical enablement (preferred). #LI-HYBRIDPlease visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity EmployerOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Director, Technical Operations Drug Product

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Job Purpose The Executive Assistant provides high-level executive administrative support to senior Operations, Quality, and Supply Chain leadership while ensuring the effective day-to-day management of the Cytokinetics Dublin office. Operating within a regulated pharmaceutical environment, the role supports governance, compliance, and business continuity through professional coordination of executive activities, facilities management, and stakeholder engagement. Responsibilities Executive &amp; Administrative Support Provide comprehensive PA and administrative support to the senior leaders based in the Cytokinetics Dublin office VP External Manufacturing, Senior Director Quality, and members of the Operations, Quality, and Supply Chain leadership teams as required, including: Proactive diary and calendar management, including scheduling of internal and external meetings. Drafting, typing, and preparation of correspondence, presentations, technical reports, memos, and briefing materials. Screening, prioritization, and management of email communications. Handling confidential information and correspondence with discretion and professionalism. Supporting the development of meeting agendas and collation of associated documentation. Expediting matters on behalf of senior management, including sourcing information, tracking actions, and following up with stakeholders. Ensuring continuity during the absence of senior leaders, including appropriate referral or escalation of matters. Governance, Meetings &amp; Business Coordination Responsibilities include agenda preparation, document collation, meeting logistics, action tracking, and follow-up. Oversee and coordinate key governance and leadership forums including: Cytokinetics Ireland Board materials. Operations Quarterly Business Reviews and weekly meetings Co-ordinate Global Supply Chain and Technical Operations meeting when held in Dublin. Travel, Events &amp; External Engagement Organize complex domestic and international business travel, including Concur management. Coordinate meetings, conferences, and workshops, both on-site and off-site, including accommodation and logistics. Facilitate arrangements for external visitors, including international visitors. Act as a professional interface with external contacts and service providers across a full range of business matters Office Coordination (EA Scope Only) Provide light oversight to ensure the Dublin office runs smoothly, in partnership with Facilities and EHSS: Interface with service providers (e.g., facilities, security) as needed. Manage office supplies and space coordination. Oversee local administrative purchasing and Oracle processing. (Note: This section is intentionally scoped as coordination, not full office‑management ownership.) Business Support &amp; Stakeholder Interaction Act as a key support and coordination point for effective collaboration with: Global Supply Chain and Technical Operations administrative teams Corporate administrative teams for Global event planning European administrative teams to ensure coordination HR Business Partner for engagement activities Senior Administrative Assistants (US &amp; Europe) Internal and external stakeholders across the organization Engages with the Cytokinetics Ireland Limited, Board of Directors when appropriate Requirements Technical Competence and Knowledge Leaving Certificate and 10+ years of relevant experience Proficient with MS Office, Concur, Budget and Procurement systems Models’ customer service, organization and professionalism. Demonstrates strong organizational skills with sharp attention to detail Completes research and tasks based on knowledge Applies knowledge from industry best practices Uses discretion and honors confidentiality with sensitive information #LI-HYBRIDPlease visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity EmployerOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Executive Assistant

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. As a key leader in the Market Access and Pricing function, the Head of Market Access for Spain and Portugal will drive the strategy, planning, and execution of market access initiatives to support the successful launch of Aficamten in 2026. Reporting to the General Manager for the territory with a dotted line to the Head of Market Access Europe, this role will focus on achieving optimal pricing and reimbursement outcomes while ensuring patients have timely access to Aficamten. This role demands strong cross-functional collaboration with medical affairs, commercial. As the Head of Market Access for Spain and Portugal, you will lead and execute strategies that ensure optimal market access, pricing, and reimbursement to support the successful launch of Aficamten across the cluster. Additionally, you will develop and implement comprehensive external engagement initiatives to build trust with key stakeholders, including payers, policymakers, and health authorities, while fostering a favorable policy environment. This position requires strategic vision, excellent cross-functional collaboration, and the ability to influence external decision-making to secure timely and equitable patient access to innovative therapies. Responsibilities Strategic Planning and Implementation Develop and implement national market access strategies tailored to the Spanish and Portuguese healthcare systems, ensuring alignment with the European Market Access Plan. Lead the development of value propositions and evidence packages to support favorable Health Technology Assessment (HTA) outcomes and reimbursement decisions with bodies such as&nbsp;AEMPS and MoH in Spain,&nbsp;INFARMED in Portugal. Pricing responsibilities will include pricing assumptions and scenarios for business review and development for the Regional &amp; Global Pricing committee when needed Oversee the planning and execution of pre-launch and launch market access activities. Drive successful launch readiness activities, including reimbursement and pricing negotiations with key stakeholders. Develop and implement regional and hospital market access strategies tailored to each healthcare system in every region in Spain. Monitor and adapt strategies based on changing healthcare systems and regulatory landscapes and implement to minimize price reductions or price reference range Stakeholder Engagement Establish and nurture relationships with key external stakeholders, including payers, policymakers, HTA bodies, and other decision-makers across Spain and Portugal. Represent the company at national and regional payer advisory boards, industry associations and working groups. Act as a company spokesperson during strategic engagements with payers and policymakers, ensuring alignment of market access narratives across all geographies. External Engagement &amp; Government Affairs Develop and implement external engagement strategies to address policy and regulatory challenges specific to Spain and Portugal. Actively monitor legislative and regulatory developments impacting the pharmaceutical industry, providing recommendations to adapt the company’s strategies. Engage with government bodies, trade associations, and patient advocacy groups to advocate for innovation-friendly policies and equitable access to healthcare. Enhance the company’s reputation by positioning it as a trusted partner within the healthcare ecosystem in both Spain and Portugal. Evidence Generation and Communication: Collaborate with HEOR to design and execute real-world evidence and economic models addressing national and regional payer requirements. Ensure clinical and economic evidence is effectively communicated through local adaptations of global dossiers and presentations to HTA and payer audiences. Review and provide input into country-specific reimbursement submissions and supporting materials. Cross-Functional Collaboration: Work closely with Medical Affairs, HEOR, and Commercial teams to align access strategies and messaging local, EU and global levels. Partner with the General Manager Spain and Portugal to define and execute country-specific goals and strategies. Support internal training and knowledge sharing on market access topics for local teams. Operational Oversight: Manage local market access budgets and allocate resources effectively to meet strategic priorities. Monitor and report on the regulatory, reimbursement, and competitive landscape to inform strategic decision-making. Ensure compliance with all local and global regulatory and ethical guidelines in all market access activities. Ensure pipeline products are appropriately included in country level horizon scanning processes. Qualifications Advanced degree in health economics, public health, life sciences, or a related field; MBA or equivalent preferred. A minimum of 7 years of experience in market access, pricing, or health economics roles within the pharmaceutical industry and regional or national payers, with significant experience in the Spanish market. Demonstrated expertise in navigating complex healthcare systems, including HTA processes and payer negotiations in Spain and Portugal. Experience in public affairs and government relations in Spain and Portugal Proven ability to manage external stakeholder networks. #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Senior Director, Market Access Spain & Portugal

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Job purpose As the Associate Director, External Manufacturing and Supply Operations, you are responsible for operational execution of external manufacturing and related supply activities. This is a central role within Manufacturing and External Supply Operations and requires the ability to manage multiple activities simultaneously, balancing priorities, with a strong sense of urgency, ability to work with ambiguity, and attention to detail. This position will have you collaborating with other members of Supply Chain, Quality Assurance, Regulatory Affairs, and Finance to execute and deliver endorsed global supply plans for both clinical and commercial supply. You will report to the Director, External Supply Operations. Responsibilities Build and maintain productive relationships with external contract manufacturers (CMO’s), and internal global colleagues Ensure timely and effective execution of all manufacturing and supply plans at assigned CMO’s Develop and manage production processes to support operational execution, including BOM’s, specifications, CAPA’s, change controls, master data, and artwork. Familiarity with ERP/MRP systems Support logistics, transportation and import/export activities Act as the manufacturing and supply chain representative for review and approval of documentation including but not limited to batch records, BOM’s, specifications, artwork, and change control Support product qualification activities including but not limited to reviewing/approving IQ/OQ/PQs, stability, and validation protocols; review and approve change controls Play a key role in supporting selection and onboarding of new CMOs, technical transfers, operationalizing product supply and site establishment Manage and track inventory, perform inventory reconciliations, and support month end close process. Issue purchase orders, and track invoices and budgets Maintain production schedules and track batch record execution in coordination with Quality Oversee, review, and approve as necessary revisions to manufacturing cGMP and non GMP documentation Proven risk management acumen with a continuous improvement mindset Where necessary, provide input to the manufacturer and QA for evaluation of process deviations and assist in the investigation of product complaints Build and maintain strong partnerships and provide effective communication with all internal and external stakeholders and lead discussion, problem solving efforts and process improvements to ensure that performance targets are met or exceeded Responsible for scheduling and maintaining routine business operations meetings with CMO’s Support Regulatory submissions and CMC as required Qualifications Education &amp; Core Experience BS/BA Degree in Life Science, Biology, or Engineering discipline from an accredited college or university, or equivalent desired 10+ years’ combined experience in manufacturing, outsourced operations, technical operations and/or supply chain in regulated healthcare industry, preferably within biotech/pharmaceutical industry cGMP career experience embedded in a pharmaceutical manufacturing plant is essential – with first-hand knowledge of plant operations, with the insight to assess performance, and diagnose issues directly at the source Technical background with knowledge of engineering and pharmaceutical manufacturing processes in small molecules is required, and experience in DS/API production is desirable Excellent problem-solving skills, with the ability to address complex challenges under time pressure Demonstrated expertise in risk management, with a history of successfully implementing risk mitigation strategies Hands-on investigations/RCA (OOS/OOT/deviations) and continuous improvement at external sites The ability to function in a fast-paced, high-growth, entrepreneurial environment Ability to travel domestically and internationally ~25% Position requires a strong working knowledge and understanding of both regional and international regulations by government agencies affecting the pharmaceutical industry (CFR's, EU GMP, ICH) Timely and effective communication across multiple audiences, both verbally and in writing#LI-HYBRID Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Associate Director, External Manufacturing and Supply

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.The Associate Director, HR Operations &amp; Total Rewards, will lead HR operational excellence across Cytokinetics’ European affiliates. This role works collaboratively with global colleagues in HR, Finance, and external partners to enable our company to best support our colleagues in Switzerland, Italy, Spain, France, Benelux, the UK, Ireland, and Germany, Austria and the Nordics. This role reports into our Head of HR, Europe. The ideal candidate combines strong technical HR expertise, total rewards knowledge, systems orientation (Workday is a plus), and a service-driven mindset. This individual will play a critical role in ensuring operational rigor, regulatory compliance, and continuous improvement across our global, regional and local HR processes. Key Responsibilities 1. HR Systems &amp; Operations System of Record Ownership: Maintain the HRIS (Workday) as the single source of truth, ensuring accurate and timely manual data entry and ongoing data integrity across all employee records. Data Governance: Implement and maintain data quality standards, performing regular audits to ensure alignment between HRIS, payroll providers, and Finance systems. Process Optimization: Identify inefficiencies in HR workflows and design improved processes to reduce manual effort, email traffic, and administrative burden. Cross-Functional Collaboration: Work closely with HR Business Partners, Talent Acquisition, Finance, Global CoEs and IT to ensure seamless data flow and operational excellence. Employee Support &amp; Escalation: Act as the escalation point for complex employee inquiries related to pre-payroll, benefits, and time-off balances, resolving issues with professionalism and a service-oriented approach. Continuous Improvement: Drive system enhancements, automation opportunities, and operational best practices to scale HR infrastructure in alignment with company growth. 2. European Payroll Coordination &amp; Data Quality Pre-Payroll Management: Own the end-to-end preparation of monthly payroll inputs for all European entities, including new hires, terminations, compensation changes, bonuses, equity events, and leaves of absence in close coordination with local HR Partners and Finance. Data Verification: Collate, audit, and validate payroll-related data to ensure completeness, accuracy, and timely submission to external payroll providers. Finance &amp; Provider Partnership: Serve as the primary liaison between HR, external payroll vendors, and internal Finance. Ensure providers receive accurate instructions on schedule and that Finance has the required documentation and reporting for approval. Audit &amp; Validation: Partner with Finance to review and validate preliminary payroll reports (gross-to-net reconciliation), identifying and resolving discrepancies prior to final pay authorization. Compliance Oversight: Ensure payroll processes comply with applicable European labor laws, tax regulations, and reporting requirements. 3. Compensation, Benefits &amp; Total Rewards Benefits Administration: Manage day-to-day administration of European benefit programs (pension, private health, life insurance, and other local benefits), ensuring accurate enrollment, termination, and vendor coordination. Vendor &amp; Broker Management: Partner with brokers and local leadership on annual benefit renewals, benchmarking, and harmonization efforts to ensure competitive and cost-effective offerings across the region in coordination with Global CoE and local HR partners. Tax &amp; Regulatory Advisory: Provide guidance on tax implications of compensation elements such as company cars, remote work arrangements, allowances, and other benefits in kind (e.g., UK P11D and comparable regional requirements). Policy Implementation: Ensure consistent execution of total rewards policies while accommodating local regulatory requirements. Data Analytics &amp; Reporting: Maintain accurate compensation and benefits records to support audits, financial reporting, and workforce analytics. &nbsp; Minimum Qualifications Bachelor’s degree in Human Resources, Business Administration, Finance, or related field. 8+ years of progressive HR operations experience; global experience supporting countries such as Switzerland, Spain, Italy, France, UK, Ireland, or Germany preferred Strong knowledge of European payroll regulations, employment law fundamentals, and benefits compliance requirements. Experience advising on tax implications of compensation elements (e.g., benefits in kind, P11D reporting, allowances, company vehicles). Proven experience managing HRIS platforms (Workday preferred) and maintaining high standards of data integrity. Strong analytical skills, pragmatic and well structured. Strong project management ability (risk assessment, stakeholder management, resource management) Experience partnering cross-functionally with Finance and external vendors. High attention to detail with the ability to manage multiple deadlines across countries. Excellent communication skills and a customer-focused approach to employee support. #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Associate Director, HR Operations and Total Rewards, Europe

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.The Director, HR Business Partner North West Europe serves as the strategic HR partner for France, Benelux, UK and Ireland, supporting the company’s first EU commercial launch planned for 2026–2027. Reporting to the Head of HR, Europe with dotted line to VP, GM France &amp; Benelux, this role is responsible for shaping and executing the full end-to-end HR agenda for the region, ensuring organizational readiness, leadership capability, and cultural alignment as the business scales. This position operates within a newly evolving European HR operating model and works in close partnership with business leaders, the European HR team, and global HR Centers of Excellence (CoEs) to deliver consistent, high-impact people solutions while addressing local market needs. Responsibilities Serve as the primary HR partner and steward of the full HR agenda for the NWE region, ensuring alignment with European and global business objectives. Partner with senior business leaders to drive performance, organizational capability, and commercial launch readiness, providing strategic counsel through periods of growth and change. Act as a trusted advisor to leaders, influencing decision-making and reinforcing the desired leadership culture and ways of working. Co-own and drive talent, organizational effectiveness, and culture-building initiatives aligned with European and global HR strategy. Lead workforce planning, organizational design, role creation, and headcount planning to support near- and long-term business growth. Support succession planning, leadership development, and long-term talent strategies to ensure leadership continuity and bench strength. Own staffing plans and recruiting pipeline quality for the NWE region, partnering closely with Talent Acquisition and HR Centers of Excellence to deliver high-quality hiring outcomes. Participate in hiring decisions for critical and leadership roles, ensuring alignment with capability, culture, and future-state organizational needs. Lead annual performance management processes, including goal setting, performance reviews, calibration, and development planning. Manage salary and bonus cycles in alignment with regional reward frameworks and corporate guidelines. Coach managers on performance planning, career development, and effective leadership behaviors, building leadership capability across the organization. Ensure consistent deployment of HR systems, policies, reward programs, and people processes in alignment with European and corporate standards, while addressing local requirements. Implement and sustain HR initiatives delivered by HR Centers of Excellence, ensuring effective adoption and change management at the local level. Contribute to European and global HR projects and cross-functional initiatives, representing NWE business needs and perspectives. Develop and execute the annual HR Business Plan aligned with European HR priorities and business objectives. Provide support for HR administration management as required, ensuring compliance, efficiency, and a positive employee experience. Qualifications 10+ years of progressive HR Business Partner or HR Generalist experience with increasing scope, complexity, and leadership responsibility In France with exposure to UK. Bachelor’s degree in Human Resources, Business Administration, or a related field; advanced degree (Master’s or MBA) preferred. Biopharmaceutical or pharmaceutical industry experience strongly preferred, ideally within a commercial environment. Proven success as a strategic HR partner in a build-out, scale-up, or first-market commercial launch environment. Demonstrated experience partnering effectively with HR Centers of Excellence in a global, matrixed organization. Deep knowledge of French labor law, unions and works council engagement; experience supporting French and UK based employee populations required. Familiarity with Belgian and/or Dutch regulations is a strong asset. Strong consulting, communication, and influencing skills, with the ability to operate credibly with senior leaders and cross-functional stakeholders. Experience operating across multiple countries and cultures, with sensitivity to regional and local market dynamics. Strong business acumen with the ability to translate business strategy into people and organizational solutions. Demonstrated change leadership capability, including experience leading organizations through growth, transformation, or ambiguity. Experience leveraging HR systems and tools, such as HRIS (e.g., Workday or equivalent), performance management and talent platforms, compensation planning tools, and workforce analytics, to inform decision-making, ensure compliance, and drive scalable people processes. Fluency in French and English. #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Director, HRBP North West Europe

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.We are currently seeking a Senior Manager, Supply Chain and Technical Project Management in our Global Supply Chain &amp; Technical Operations department.&nbsp; This position is integral to the advancement of Cytokinetics’ growing portfolio of drug candidates and technology programs and will coordinate cross-functionally to ensure project deliverables are met on-time, on-budget, and with a high degree of quality. Reporting to the Director of Portfolio Management within Global Supply Chain &amp; Technical Operations, this role will be responsible for the creation, and management of timelines, and deliverables to support the technical development, validation, and commercialization of drug substances, formulated drug product and packaging using Cytokinetics internal resources and an external network of providers.&nbsp; Responsibilities Provide project management support at any stage of the drug development lifecycle (e.g., early to late-stage development, market authorization, or post-launch phases) Develop charters, integrated schedules, deliverable lists, status updates, resource requests and related communications for assigned projects and programs Maintain a positive, results-oriented work environment by building partnerships, modeling collaboration and communicating in an open, balanced and objective manner to enable a high-performing team Proactively monitor timelines, KPIs, critical path, and resources for assigned projects using appropriate tools, project management principles and practices to deliver project objectives Work cross-functionally to coordinate interdependencies with other projects. Resolve and/or escalate conflicts and issues to remove barriers to project success Leverage risk management tools and techniques to proactively identify, mitigate and manage risks throughout the project lifecycle to avoid deviations to the project goals and objectives Engage sponsors, functional senior leadership, and key stakeholders in regular and meaningful project communications (dashboards, reports, metrics, etc.) to ensure delivery of expected business outcomes Lead and/or support continuous improvement of processes and tools 10-20% Travel, as necessary according to project needs Qualifications BA/BS in Scientific, Technical, Engineering or Business discipline (advanced degree preferred) A minimum of 10 years total work experience, with at least 5 or more years relevant experience in project management within the life sciences (pharmaceutical / biotech / medical device) industry Sound technical knowledge in one or more of the following categories: Chemical Development, Formulation Development, Clinical, Manufacturing, Analytical, Packaging, Serialization, Planning, or Logistics (small molecule drug development is a plus) Outstanding project management, planning, organization, prioritization, and time management skills Ability to adapt to changing situations, and effectively manage multiple projects and priorities Ability to think creatively in order to provide non-standard solutions Strong partnering skills – ability to thoughtfully cultivate strong and highly effective working relationships with internal and/or external customers and stakeholders Strong influencing, organizational and interpersonal skills – consistently achieves targeted results without authority by leveraging expertise, business knowledge, and partnerships Project Management Professional (PMP) Certification preferred Six Sigma or other Operational Excellence related certifications is a plus#LI-HYBRID Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Senior Manager, Supply Chain & Technical Project Management

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.The Associate Director International FP&amp;A reports to the Head of International Finance and serves as an integral member of the International Finance team. The position will have a dotted-line reporting relationship to the US-based FP&amp;A team. The role serves as a key advisor to the EU Heads of Functions (Commercial, Medical Affairs, Regulatory, G&amp;A, Supply Chain, and Quality) and contributes to the organization’s development and achievement of strategic goals. This is an outstanding opportunity for a senior finance professional with operational experience and a proven track record of creative problem-solving and change management to join a high-growth, patient-centric, mission-driven organization. Duties and Responsibilities: Planning / Resource Allocation and Optimization Act as a key advisor to the Heads of Functions within the International region to drive results aligned with corporate strategy and goals. Develop and implement forward-looking financial analytics to provide insights into operations and business plans. Maintain continuous communication with the Head of Finance International and Sr. Director FP&amp;A Global Supply Chain / Tech Ops regarding critical issues. Provide day-to-day finance support for the Ireland supply chain operations site, including analysis of global manufacturing contracts, purchase orders, and headcount reporting. Support annual budget, quarterly forecast, and long-range planning processes for supply chain and operations-related cost structures. Plan, coordinate, and execute the annual budget and forecast process for all relevant functions. Prepare regular reporting packages and presentations for senior management highlighting financial performance and risks. Support long-range planning activities. Manage quarter-end and year-end accruals, consolidation, and reporting of quarterly financials. Perform monthly variance analysis between forecast, budget, and actual results, identifying key drivers and recommending corrective actions. Coordinate cross-functionally across the International region. Ensure compliance with internal controls and procedures. Participate in or lead special projects. Perform other duties as assigned by management. Team Development / Leadership Promote a culture of high performance, accountability, and continuous improvement. Lead by example and communicate effectively across functions. Qualifications: Bachelor’s degree required; MBA preferred. 8–10 years of experience in financial leadership roles, preferably in the pharmaceutical or biopharma industry. Experience directly supporting senior Commercial and Manufacturing executives. Strong knowledge of financial planning, accounting, and cost accounting. Excellent written and oral communication skills in English. Demonstrated leadership ability, team management, and interpersonal skills. Strong financial modeling, analytical, and abstract reasoning skills. Ability to operate effectively as both a tactical and strategic thinker. Experience with ERP systems (SAP, Oracle, NetSuite) and planning tools. Advanced Excel skills. #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Associate Director International FP&A

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.The Senior Accounting Manager, DACH, reporting to the Head of International Accounting, plays a pivotal role within the International Finance team. This position oversees statutory and tax compliance for the DACH region (specifically Germany and Switzerland) and ensures robust SOX and US GAAP compliance. It offers an exceptional opportunity for an experienced finance professional with hands‑on operational capabilities and demonstrated success in developing and strengthening finance organizations. Duties and Responsibilities: Statutory &amp; Financial Reporting Lead preparation and filing of statutory financial statements for all DACH legal entities under local GAAP Coordinate year-end statutory reporting and disclosures Ensure compliance with local accounting standards and regulatory requirements Manage statutory adjustments from group reporting to local GAAP Coordinate with external advisors for statutory accounts and filings Maintain statutory accounting calendars and ensure deadlines are met Partner with the External Accounting Firm Audit Management Act as primary contact for external auditors across DACH entities Manage statutory audits end-to-end, including planning, documentation, and issue resolution Coordinate internal audit requests and remediation actions Prepare audit schedules and supporting documentation Ensure timely closure of audit findings and control deficiencies Support SOX / internal control compliance (partnering with US team) VAT Responsibilities Oversee preparation and timely submission of VAT returns and related filings across all DACH entities, in coordination with internal tax teams and external advisors Ensure accuracy and completeness of VAT reporting through reconciliation of VAT accounts to the general ledger Review VAT treatment of complex transactions, cross-border supplies, and intercompany charges Support VAT audits and inquiries from tax authorities, including documentation and response coordination Monitor changes in VAT legislation and ensure accounting processes and controls remain compliant Balance Sheet Governance Own balance sheet integrity across all DACH entities Ensure timely and accurate balance sheet reconciliations for all accounts Prepare reconciliations Investigate and resolve aged or unusual reconciling items Drive continuous improvement in balance sheet control processes Compliance &amp; Regulatory Ensure EU entities operate in full compliance with US GAAP, corporate accounting policies, and SOX internal control requirements Own and maintain SOX control framework across EU entities, including documentation, control design, and operating effectiveness testing Partner closely with US Corporate Accounting, Internal Audit, and Controllership teams to support quarterly and annual SOX certifications Coordinate remediation of control deficiencies, ensuring timely resolution and sustainable process improvements Qualifications: A minimum of a BS or similar designation; CPA preferred Minimum 10 years of progressive accounting experience, including statutory reporting and financial close for multiple EU entities, preferably within a multinational environment Strong expertise in US GAAP reporting, with solid knowledge of local GAAP requirements across European jurisdictions, mainly Germany and Switzerland Proven experience managing external and internal audits, including SOX compliance, internal controls, and audit coordination with Big4 or international audit firms Demonstrated experience in balance sheet governance, reconciliations, and month-end/quarter-end close processes in a complex multi-entity structure Ability to partner effectively with US Corporate Accounting and Controllership teams, ensuring alignment with global accounting policies and reporting deadlines Advanced proficiency in Microsoft Excel, including complex formulas, pivot tables, data analysis, and financial reporting models Strong experience working with ERP systems such as Oracle, SAP, NetSuite, or similar financial systems Experience with financial consolidation and reporting tools (e.g., Oracle Hyperion or similar platforms) Solid understanding of general ledger systems, account reconciliation tools, and automated close processes Ability to analyze large financial datasets, improve reporting automation, and leverage financial systems to enhance accounting processes and internal controls Language skills: English fluent, and German preferred LI-HYBRID Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Senior Accounting Manager, DACH

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Job purpose This role supports Cytokinetics European Countries across all functional areas and is responsible for procuring goods and services at the Country level. &nbsp;The Sr. Procurement Operations Specialist (Contract) is accountable for working with internal and external partners to optimize purchasing activities and assessing and communicating challenges, risks, opportunities, and decisions with skill and diplomacy. Responsibilities Provides oversight of externally contracted activities at the Country level; demonstrates ability to engage technically, operationally and commercially to enable Procurement activities. Solicits and analyzes requests for proposals, negotiates contracts, and ensures contract objectives are realized (savings, SLAs, etc.); ensures compliance with pricing agreements and internal policies/procedures. Performs administrative tasks including initializing purchase orders and management of document flow between various functions related to RFIs, RFPs, and contracts (e.g. MSAs, Work Orders, Change Orders, Consulting Agreements, etc.) Gains proficiency in Linksquares, responsible for input and oversight of document workflow in the legal contract system. Responsible for tracking all vendor contract requests, providing regular follow-up to ensure timely approval, and maintaining vendor documentation. Manage purchasing activities to ensure goods are within delivery, quality, compliance, and pricing parameters. Manage supplier relations and performance, including vendor selection, vendor set up, pricing negotiation, invoicing, returns/credits, and on-time delivery. Develop and implement policies and procedures related to purchasing with a goal of maximizing efficiency and optimizing workflow. Qualifications Minimum BA/BS / University Degree 7+ years of experience of supply chain / purchasing / procurement experience Experience using an ERP system (Oracle Fusion preferred) Demonstrated experience in electronic contracts management systems Ability to work effectively and efficiently with all levels of management and personnel Ability to handle multiple projects in a timely manner Strong commitment to customer service Demonstrates ability for problem-solving in collaboration with internal and external contacts Demonstrates excellent verbal, written, and interpersonal communication skills; professional manner Strong organizational and planning skills and meticulous attention to detail Able to work independently while exercising initiative, flexibility and good judgment#LI-HYBRID Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Sr. Procurement Operations Specialist (Contract)

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. We have the flexibility to offer this position either on Sr Specialist or on Associate Director level, to be adjusted to the experience of the successful candidate. The Cardiovascular Therapeutic Area (CV-TA) Senior Specialist/Associate Director, Medical Affairs will assume a key role within the organization, will work collaboratively with other members of the Medical Affairs team in the development and execution of the Medical Affairs plan for aficamten as well as collaborate cross-functionally with the Commercial and Clinical departments in the strategic planning and life-cycle management process of our cardiovascular portfolio. The Senior Specialist/AD will provide support to internal colleagues, resolve medical issues, and provide critical input into the development of medical documents (external scientific communications, standard response letters, training materials, product materials, publications, research ideas, internal training materials, etc.) to ensure high strategic and scientific standards. Importantly, the Sr. Specialist/AD will serve as a key member of the Medical Affairs Hypertrophic Cardiomyopathy team, may represent Medical Affairs externally through presentations at advisory boards, key scientific meetings, and interactions with our key investigators. Additionally, the Sr Specialist will support strategic partnerships with key opinion leaders, academic institutions, and professional societies. Responsibilities Supports the development of aficamten, including Assists in development of strategic planning, Execution of medical launch activities, Education of healthcare practitioners and internal teams regarding the clinical profile of aficamten and its place in HCM therapy Support the Medical Affairs review of medical and promotional scientific materials related to hypertrophic cardiomyopathy and aficamten Provide day‐to‐day medical guidance while working closely with other members of the Medical Affairs team in Zug and in Europe and cross-functionally within Cytokinetics and with external business partners. Activities include: Participation in appropriate cross‐functional and cross‐company Medical and Commercial teams to inform brand strategies and tactics and represent Medical Affairs Clinical and scientific support in responding to inquiries from healthcare professionals Scientific congress/conference strategy and planning, advisory boards, publication steering committee meetings, field force training, review of medical information standard response letters, and marketing/policy related projects. Input into medical education, grant, and sponsorship review Scientific input into publication strategy for the hypertrophic cardiomyopathy therapeutic area, including review of abstracts and posters for presentation at scientific meetings and manuscripts for publication Help develop integrated evidence plan (IEP) strategy including life cycle management through leading workstreams to identify evidence gaps and establishes linkage between Medical, Research and Development (R&amp;D), HEOR to develop data generation. Support scientific and clinical priorities for an investigator sponsored study program as we near launch and support the internal review committee that adjudicates submitted research proposals. Present data at company advisory board meetings and training programs. Help identify and effectively interact with hypertrophic cardiomyopathy external experts to engage in scientific exchange to meet the needs of patients and the medical community. Qualifications PharmD/PhD/MD with prior pharmaceutical industry experience preferred (+1 year for Sr. Specialist, and more for AD level). Proven ability to work independently and as a member of an integrated, interdisciplinary team in carrying out assigned responsibilities Must be analytical and articulate in both oral and in writing skills, possess excellent presentation skills, with a demonstrated ability to communicate well with others at varying professional levels Background in academic medicine, clinical research, and familiarity with biostatistics and epidemiology highly desirable A history of clinical or research collaboration with opinion leaders in the CV-TA is preferred Familiarity with EFPIA, PhRMA code, and key regulations in the pharmaceutical industry a plus Proficiency with Microsoft Office Knowledge of other European languages beyond English highly desirable Ability to travel domestically and internationally (~20% of time) #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Senior Medical Affairs Specialist

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. We are seeking an experienced Payroll Manager to support our growing organization. This role will be responsible for overseeing payroll operations, ensuring accuracy, compliance, and efficiency across processes while partnering closely with internal stakeholders and external providers. This is a fixed-term contract until the end of the year, with the possibility of extension. The position follows a hybrid working model, with three days per week in our Zug office. Key Responsibilities: End-to-End Payroll Operations: manage and oversee full-cycle payroll processing for EU entities, ensuring accuracy, completeness, and timely salary payments in compliance with local labor and tax regulations. Partnering with HR and BDO. Process manual payment for newly created entities. Balance Sheet Reconciliations: own payroll-related balance sheet accounts for all EU entities, including salaries payable, social security liabilities, bonus accruals, and other employee-related provisions. Payroll Accounting &amp; Accruals including PTO / Leave Accrual Management: oversee paid time off (PTO), vacation, and leave accrual calculations; ensure compliance with local labor laws and accurate financial reporting of leave liabilities. Prepare and issue monthly PTO balance report with lead team. Review payroll-related journal entries, including salary, bonus, commission, and employer tax accruals; ensure proper reconciliation to the general ledger. Equity / Stock Compensation Process Management: coordinate payroll treatment of stock-based compensation (RSUs, options, ESPP), ensuring proper taxation, reporting, and accounting in alignment with corporate policies. Close partnership with BDO and Tax department. Validation of annual certificate required for employees. Compliance &amp; Regulatory Reporting, Internal Controls &amp; SOX Compliance: ensure timely submission of payroll tax filings, social security contributions, and statutory reports in coordination with local authorities and providers. Maintain and strengthen payroll-related internal controls, support SOX documentation and testing, and ensure audit readiness for both internal and external audits. Accounting Manager responsibility for France entity, FBNL protentional (approximately 30% of time). Lead preparation and filing of statutory financial statements for France legal entities under local GAAP. Oversee preparation and timely submission of VAT returns and related filings across all France, in coordination with internal tax teams and external advisors. Own balance sheet integrity across all DACH entities. Qualifications: Minimum 10+ years of progressive experience in end-to-end payroll management, with strong expertise in multi-country or multi-state compliance, tax regulations, statutory reporting and benefits administration. Proven ability to implement, optimize and scale payroll systems and processes. Demonstrated capability to design and manage agile payroll frameworks within fast-paced, high-growth or startup-style environments, partnering closely with Finance, HR, and leadership teams. Excellent communication, stakeholder management, and leadership skills, with experience mentoring team members and building trusted cross-functional relationships in dynamic organizational cultures. Fluency in English (written and spoken) is required to effectively manage global payroll communications, documentation and stakeholder coordination. Additional proficiency in relevant regional languages (e.g. French) is strongly preferred. Clear and professional written communication skills for reporting, policy documentation, and audit-related correspondence. &nbsp; #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Payroll Manager (Contractor), 100%

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.As a subject matter expert in Medical Affairs, the Senior Director Medical Affairs UK will oversee all medical initiatives throughout the UK and contribute to the development and implementation of global medical affairs strategies. They will provide support to internal colleagues and collaborate closely with the Global &amp; European Medical Affairs teams to ensure high strategic and scientific standards by resolving medical issues and providing critical input in the development of medical documents (publications, external scientific communications, standard response letters, product materials, research ideas, internal training materials, etc.). The Medical Director, under the guidance of the VP of Medical Affairs Europe to whom s/he will be reporting (and dotted line to the UK leader), will ensure strategic partnerships with key external opinion leaders and academic institutions in the UK market, and represent Medical Affairs externally through presentations at advisory boards, key scientific meetings, and interactions with our key investigators.&nbsp; In addition, the Medical Director will work cross-functionally with other colleagues to provide expertise on varied workstreams, including pre-launch and launch activities related to late-stage assets. &nbsp; The role is hybrid twice per week in London office.&nbsp; Responsibilities Serves as an integral component of the Medical Affairs contribution to the UK launch of our late-stage cardiovascular clinical compounds, including: Implementation of the Country Plan of Action based on the Global and European Medical Affairs Plan, Execution of medical pre-launch and launch activities, Education of Cardiovascular HCPs (heart failure and hypertrophic cardiomyopathy) regarding the clinical profile of our CV compounds and their place in therapy Can speak to the mechanism of action of the compounds and their development, including Phase I-IV studies, at a detailed scientific level in a reactive conversation with key opinion leaders. Provide day‐to‐day medical guidance while working closely on joint projects with other members of the Medical Affairs team, the Countries leadership, other departments internally and our business partners. Projects may include scientific congress/conference strategy and planning, advisory boards, field force training, review of medical information standard response letters, health economics and epidemiology analyses, and marketing/policy related projects. Represent the company at Medical Congresses and ensure Medical Affairs coverage, including scientific session attendance and reporting, and information booth support. Represent the company in patient groups and associations. Provide scientific input into publication strategy and review abstracts and posters for presentation at scientific meetings and manuscripts for publication. Participate in appropriate cross‐functional and cross‐company Medical and Commercial teams in the UK to inform brand strategies and tactics and represent Medical Affairs. Liaise with Global &amp; European Medical Affairs and R&amp;D colleagues to develop and maintain timely and relevant product expertise for the region. Provide input into medical education, grant, and sponsorship review. Provide clinical and scientific support in responding to inquiries from healthcare professionals. Participate as medical reviewer in the Medical Review Committee and the Promotional Materials Review Committee Data Generation and Presentation Present data at company advisory board meetings and training programs Collaborate with R&amp;D and HEOR in data generation projects to address identified medical data gaps for the UK Help identify and effectively interact with opinion leaders to engage in scientific exchange to meet the needs of patients and the medical community. Collaborate with Market Access and the HEOR function to define research strategy and design of studies, including the generation of real-world evidence and cost-effectiveness analyses. Provide support for and collaborate with the field medical teams in the UK and support reactive material development to address healthcare professional inquiries. Upon initiation of a Phase 4 program, participate in the review and adjudication of investigator-sponsored study research proposals. Qualifications MD/MBBS with strong Medical Affairs experience. Cardiovascular experience preferred, clinical experience desirable. Position will be filled at a Director level (i.e. Director, or Senior Director) commensurate with experience. 7 years of pharmaceutical industry experience preferred. Medical Affairs experience in the UK (with particular knowledge of the Countries market) with medicine approvals and peri-launch and launch activities. Background in academic medicine, clinical research, and familiarity with study design, biostatistics and epidemiology desirable. Proven ability to work independently and as a member of an integrated, interdisciplinary team in carrying out assigned responsibilities. Must be analytical and articulate in both oral and writing skills, possess excellent presentation skills, with a demonstrated ability to communicate well with others at varying professional levels. Familiarity with relevant regulatory authorization requirements and other key local authorities in the regional pharmaceutical industry. Ability to think broadly about scientific communications and the impact on medical content. Business fluent in English. Knowledge of other European languages are a plus. Proficiency with Microsoft Office Ability to travel within the UK, across Europe, and internationally (~35% of time) &nbsp; #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Senior Medical Director, UK

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.The Director, Analytical Development &amp; CMC Compliance is a strategic technical subject matter expert (SME) supporting analytical development roadmap establishment, analytical process optimization, and continuous improvement. The position acts as a technical leader and subject matter expert (SME) in CMC analytical development strategy from tox to Phase 1 through Phase 3 to support global regulatory filings (IND, IMPD, NDA, MAA, etc.). Leads the development, qualification, and lifecycle management of analytical methods and control strategies aligned with ICH guidelines and evolving regulatory expectations. Ensures robust, compliant analytical control strategies to enable successful clinical progression, registration, and commercial success. The position works closely with Manufacturing, Process Development, Regulatory CMC, and Quality Assurance to ensure compliance with global regulatory standards (e.g., FDA, EMA, ICH) and to enable successful product approvals. Responsibilities Technical Leadership Execute analytical development strategies aligned with corporate objectives, program requirements, Analytical Target Profile (ATP) and Quality Target Product Profile (QTPP), in close collaboration with line management and GSC&amp;TO leadership. Lead establishment and maintenance of Analytical Development standards, integrating all best in industry guidelines and Health Authority regulations. Drives the design and implement robust, phase-appropriate and robust analytical approaches to enable successful clinical development and registration. Provide technical leadership and mentorship, influencing cross-functional decisions and advancing analytical and compliance excellence within CMC Analytical. Serve as a technical and regulatory subject matter expert, supporting inspections and audits and contributing to inspection readiness.2. Analytical Development Lead analytical development activities of assigned programs, characterization studies, comparability assessments, and stability strategies. Manages the development, qualification, validation, and lifecycle management of analytical methods and control strategies. Manage GMP testing for raw materials, in-process, drug substance, and drug product. Oversee development activities at external laboratories and CDMOs ensuring compliance and timeline. Lead analytical transfer activities supporting drug substance and drug product manufacturing process transfer and scale up. Serve as analytical subject matter expert in due diligence activities. Ensure timely release testing and stability testing to meet development and production timelines. Manage change control, OOS/OOT investigations, CAPA implementation, and deviation management. Ensure compliance with ICH guidelines (e.g., Q2, Q14), USP, EP, JP &nbsp;and other compendial standards. Support regulatory submissions (IND, IMPD, NDA, MAA, JNDA, etc.) including authoring/ reviewing high-quality CMC sections and lead responses to regulatory questions (RTQs). &nbsp; &nbsp; &nbsp;3. Quality &amp; Regulatory Compliance Serve as Analytical method and Quality Control SME during regulatory inspections (e.g., FDA, EMA, PMDA). Support inspection readiness and continuous improvement culture. Ensure data integrity and GMP documentation practices. &nbsp; &nbsp; &nbsp;4. Budget &amp; Resource Management Support development and execution of program budgets (capital and operational). Optimize internal vs. external testing strategies. Evaluate and implement advanced analytical technologies. Qualifications Education Ph.D. or equivalent in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or related field (preferred) Experience 10+ years in pharmaceutical/biotech analytical development with demonstration of progressive technical leadership roles and global experience Demonstrated experience supporting INDs, NDAs/MAAs Demonstrated experience with stage gate development strategies. Direct experience interacting with global health authorities &nbsp;Technical Expertise Chromatography (HPLC, UPLC, GC) Mass spectrometry Stability studies and degradation pathways Method development, validation, transfer, and lifecycle management Proficient in writing technical reports and AD/QC sections of CMC regulatory documents GMP laboratory systems (Veeva, LIMS, Empower) Analytical development experience in drug substances and drug products Core Competencies Strategic thinking and enterprise leadership Strong regulatory and compliance acumen Operational excellence mindset Excellent interpersonal, communication and decision-making/influencing skills Expert knowledge of cGMP and GLP compliance and regulations and experienced in manufacturing batch record review, product specifications, stability programs and other AD/QC activities Demonstrated ability to manage external contractors to meet or exceed Company goals Risk assessment and problem-solving expertise Exceptional communication and mentorship skills#LI-HYBRID Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Director, Analytical Development & CMC Compliance

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Job purpose As a Manager, External Manufacturing and Supply Operations, you are responsible for the end-to-end technical and operational oversight of external manufacturing and supply activities across a network of Contract Manufacturing Organizations (CMOs). This role sits at the core of Manufacturing and External Supply Operations and requires a strong technical foundation, the ability to manage multiple concurrent priorities, and to operate effectively in a fast-paced, ambiguous environment. This position places particular emphasis on batch record review and approval, process oversight, and technical decision-making, ensuring that manufacturing activities are executed in full compliance with cGMP standards and aligned with global supply requirements. You will collaborate cross-functionally with Quality Assurance, Technical Operations, Regulatory Affairs, and Supply Chain to ensure robust, compliant, and reliable supply for both clinical and commercial products. You will report to the Director, External Supply Operations. Responsibilities Build and maintain strong, technically credible relationships with external CMOs and internal cross-functional stakeholders Provide hands-on technical oversight of manufacturing operations at CMOs, ensuring adherence to validated processes, regulatory expectations, and internal standards Own and lead the review and approval of batch records, ensuring accuracy, completeness, and compliance with cGMP and product specifications Act as the technical authority for batch disposition readiness and support, identifying and resolving issues that may impact product quality or release timelines Ensure prompt execution of manufacturing and supply plans, proactively identifying risks and implementing mitigation strategies Drive investigation and resolution of deviations, OOS/OOT events, and product complaints, including leading or supporting root cause analysis (RCA) and CAPA development Provide technical input and oversight for change controls, ensuring appropriate impact assessments and alignment with regulatory filings and process validation state Develop and support deep understanding of manufacturing processes (API, Drug Product, and Packaging) to enable effective troubleshooting and continuous improvement Review and approve technical documentation, including but not limited to: Batch manufacturing and packaging records Specifications and master data Validation protocols and reports (IQ/OQ/PQ) Stability protocols and reports Change controls and deviations Support process validation and ongoing process verification, ensuring continued state of control at CMOs Play a key role in technology transfers, process scale-up, and site onboarding, ensuring technical robustness and successful execution Partner with Quality and CMO teams to monitor batch execution in real time, ensuring proactive issue identification and resolution Ensure effective management of BOMs, master data, and ERP/MRP systems to support accurate production planning and execution Lead or participate in routine governance and operational meetings with CMOs, driving accountability and performance improvements Support regulatory submissions and CMC activities, ensuring technical accuracy and consistency with manufacturing processes Maintain oversight of inventory, production schedules, and supply continuity, ensuring alignment with demand and minimizing supply risk Drive a continuous improvement culture, identifying opportunities to enhance process robustness, reduce deviations, and improve right-first-time performance Qualifications Education &amp; Core Experience BS/BA Degree in Life Sciences, Engineering, or related discipline desirable 10+ years’ experience across pharmaceutical manufacturing, technical operations, or external supply in a regulated environment Strong cGMP manufacturing experience within a pharmaceutical plant environment, with direct exposure to shop-floor operations and batch execution Demonstrated expertise in batch record review and approval, with a deep understanding of critical process parameters, in-process controls, and data integrity Proven experience working with external CMOs, providing technical oversight and driving performance in outsourced manufacturing environments Strong technical knowledge across Drug Product, API, and Packaging operations, with the ability to troubleshoot complex manufacturing issues Hands-on experience in deviation management, investigations (OOS/OOT), and CAPA implementation Solid understanding of process validation, lifecycle management, and continued process verification Experience supporting or leading technology transfers and process scale-up activities Strong working knowledge of global regulatory requirements (FDA, EMA, ICH, EU GMP) Experience with ERP/MRP systems and manufacturing data structures (BOMs, master data) Proven ability to apply risk management principles and make sound technical decisions under pressure Excellent communication skills, with the ability to clearly articulate complex technical issues to diverse stakeholders Ability to operate effectively in a fast-paced, high-growth environment, managing multiple priorities simultaneously Willingness to travel (~25%) to support CMO oversight and on-site technical activities#LI-HYBRID Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Manager, External Manufacturing and Supply

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Job purpose We are seeking a Director of Packaging &amp; Artwork Management to lead the strategy, systems, and execution of artwork lifecycle management. Reporting to the VP of External Manufacturing, this role will build inspection-ready, scalable, and fit-for-purpose artwork capabilities, with a strong emphasis on Global market requirements. This role is accountable for establishing end-to-end artwork management, including system selection and validation, intake and workflow design, lifecycle processes, and regulatory alignment. The leader will operate in a fast-paced, resource-constrained environment, balancing compliance, speed, and efficiency while supporting global commercialization. Responsibilities Artwork Strategy &amp; Systems Define and implement a scalable global artwork strategy aligned to company growth. Lead selection, validation, and deployment of Artwork Management Systems (AMS), including: Ensure systems are GxP-compliant, right-sized, and integrated with Regulatory, Quality, and ERP platforms as appropriate. Intake, Triage &amp; Workflow Management Establish a centralized intake and prioritization model for artwork requests across products and markets. Implement governance and prioritization frameworks (launches, lifecycle changes, safety updates). Deploy tracking tools and dashboards to provide visibility into timelines, risks, and bottlenecks. Align artwork demand with regulatory submissions and manufacturing schedules. Artwork Lifecycle Management Design and implement end-to-end processes (creation, review, approval, change control). Enable efficient cross-functional workflows that minimize cycle time while ensuring compliance. Establish version control, audit trails, and documentation to support inspection readiness. Oversee mock-ups and concept artwork for regulatory and internal use. Safety &amp; Time-Critical Labeling Updates Build lean, rapid-response processes for safety-driven labeling updates. Ensure accelerated execution while maintaining full compliance. Coordinate with Regulatory, Pharmacovigilance, and Manufacturing to support timely multi-country implementation. Packaging &amp; External Manufacturing Integration Partner with External Manufacturing and CMOs to ensure artwork is production-ready. Align artwork processes with packaging operations, supply timelines, and launch readiness. Provide oversight to artwork vendors and packaging partners to ensure quality and consistency. Compliance, Quality &amp; Continuous Improvement Establish and maintain GMP-compliant SOPs, policies, and workflows. Ensure all activities are inspection-ready and aligned with global expectations. Drive improvements in cycle time, right-first-time performance, and process simplicity. Leadership &amp; Performance Management Act as the artwork and labeling SME across Regulatory, Quality, Supply Chain, and Commercial. Define and track KPIs (cycle time, approval timelines, right-first-time, on-time delivery). Manage budget and vendors with a focus on cost-effective, scalable solutions. Qualifications Required Experience Bachelor’s degree preferred 10+ years in pharmaceutical packaging, labeling, and artwork management within a GxP environment Demonstrated experience building artwork intake, triage, and tracking processes in fast-paced environments Track record of success implementing end-to-end artwork lifecycle management Proven success in managing time-critical labeling and safety updates and selecting and deploying validated AMS platforms Leadership Capabilities Proven ability to build scalable processes from the ground up Strong stakeholder management and decision-making skills Ability to simplify complexity and drive execution in resource-constrained settings#LI-HYBRID Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Director, Packaging and Artwork Management

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.We are seeking an experienced Director of Quality Assurance, Alliance Management to join our growing global organization. As Cytokinetics expands through strategic in-licensing partnerships with regional market leaders, this role will be critical in ensuring that all quality and compliance aspects of these partnerships are effectively established and maintained. This position will lead and coordinate Quality Assurance activities across partner relationships, ensuring alignment with global regulatory requirements and internal standards. The successful candidate will act as a key liaison between Cytokinetics and its partners, supporting both the onboarding of new alliances and the ongoing management of established collaborations. The role reports to the Head of Quality Assurance Operations and works closely with Alliance Management, Technical Operations, Regulatory CMC, and other cross-functional teams. Key Responsibilities Serve as a core member of the QA Operations team and Point of Contact (POC), coordinating quality requirements arising from partnership activities, in partnership with alliance management teams Lead and manage all Quality Assurance activities related to the onboarding of new partners Develop scalable frameworks, models, and processes for partner onboarding and QA integration Act as the lead for partner-related Quality Assurance audits Develop standards for Quality Agreements supporting in-licensing partnerships in collaboration with Quality Compliance Review and approve (as applicable) change controls, deviations, investigations, procedures, and CAPAs related to partner supply Participate in Quality Management Review meetings, providing input on partnership-related quality topics Collaborate with Quality Systems and Compliance to ensure the QMS meets market-specific regulatory requirements associated with partnerships Ensure timely and effective resolution of quality issues related to product supply for partners Conduct risk assessments and implement appropriate controls when onboarding new partners Partner with Technical Operations, Regulatory CMC, and other functions to ensure GMP compliance across new markets and partnerships Support review of Product Quality Reviews (PQRs) as part of partner oversight Represent the QA function in cross-functional and external meetings, making decisions within scope of responsibility Promote a culture of quality, compliance, and continuous improvement across the organization Identify and lead initiatives to enhance quality systems, processes, and practices &nbsp; Qualifications &amp; Experience Bachelor’s degree (BSc) or higher in a relevant scientific discipline Minimum of 10 years’ experience in pharmaceutical or biopharmaceutical manufacturing and quality functions Strong knowledge of global cGMP regulations and emerging regulatory trends Experience in a biopharma or pharmaceutical start-up environment, Preference for experience hosting regulatory inspections and/or partner/client audits Demonstrated ability to influence and collaborate effectively across all organizational levels Experience working with external partners, alliances, or contract organizations Strong ability to work independently, demonstrating initiative and sound judgment Excellent organizational skills with the ability to manage multiple priorities effectively Strong written and verbal communication skills Proficiency in Microsoft Office applications Fluency in English; additional language(s) are an advantage Willingness to travel up to 15% annually#LI-HYBRID Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Director of Quality Assurance, Alliance Management

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Reporting to the Senior Medical Director Italy, the Associate Medical Director Italy role will be customer facing with medical field team responsibility for our roll out and also be strategic, to support implementation and execution of the devised medical launch strategy for CYTK products in Italy.&nbsp; The Associate Medical Director will serve as national lead of a team consisting of scientific professionals who serve as a key field-based scientific resource for healthcare providers, patients, industry partners and internal colleagues. In this role, the individual will lead field medical operations and manage a field-based Italian Medical Science Liaison (MSL) team. The Associate Medical Director will collaborate and actively support the cross-functional team with the execution of the medical strategy in Italy and provide input relevant to our broader European efforts, based on their local expertise and insights. The Associate Medical Director will be a key role in the ongoing build out of the wider planned Italy medical affairs team. Responsibilities Subject matter expert in HCM disease state and its management in Italy as well as on aficamten and its competitors In collaboration with the Italian Sr Medical Director, strategize on the development of the country medical affairs plan and implementation of a field Medical Affairs vision and strategy, in alignment with the company’s corporate strategies and objectives. Lead field medical operations as the company’s field-based Medical Affairs team leader, participating directly in KOL/HCP development and engagement as well as supporting ongoing early and late-stage clinical trials in his region. Lead field medical launch-related planning for aficamten (a cardiac myosin inhibitor) being developed for obstructive hypertrophic cardiomyopathy (oHCM) and future new indications (if any). Ensure the MSL team is continuously trained on emerging aficamten data as it’s presented at congresses &amp; via scientific publications and incorporate such data into the MSL aficamten Communication Plan. Foster a compliant, cross-functional, customer-centric team approach between the MSL team and other Cytokinetics field-based teams/roles as the company transitions from Research &amp; Development to a Commercial organization. Manage and mentor a MSL team while providing strong leadership to develop and motivate the MSL team to meet and exceed key performance indicators (KPIs). Clearly communicate national and local MSL goals, objectives, and KPIs. Actively support the MSL team and their efforts by advocating and promoting collaboration within the team, across internal working groups, and with customers. Guide and assist the MSL team in key opinion leader and expert cardiologist engagement in the field and with internal stakeholders. Establish and maintain collaborative relationships with targeted scientific leaders to develop potential scientific and clinical therapeutic ideas related to hypertrophic cardiomyopathy (HCM) and heart failure (HF)), including coordination/support of investigator-initiated, non-registration pre-clinical and/or clinical studies. In close collaboration with international and global team establish a CRM system in Italy and being the responsible person for this in Italy Ensure that all MSL interactions and activities adhere to corporate and healthcare compliance guidance, including those related to scientific interactions with internal and external groups, responses to unsolicited requests for medical/scientific information, and discussion of external research. Collect insights from the field and sensitize the MSLs on competitive intelligence Facilitate a training strategy for disease state and portfolio/pipeline products to enhance MSL team knowledge. Maintain clinical, scientific, and technical expertise in cardiovascular medicine. Serve as a scientific resource to internal functional areas within Cytokinetics including serving as a member of cross-functional teams as required. Work with Medical Affairs and other internal, cross-functional colleagues on initiatives including congress planning, medical information, publications, medical education, and speaker training, as well as align priorities around areas of research interest. Train and organize the MSL team to effectively support congress activities like booth duty, scientific session coverage, KOL engagement, competitive intelligence collection, etc. Support planning, execution and leadership Italian advisory boards to gather feedback and input on study design, clinical trial data, clinical experience and medical education. Provide medical input and support to the commercial and market access activities for Italy Ability to travel regularly as required, region wide and globally, as necessary for business needs and development support Collaborate and work closely with all necessary related and associated departments including Marketing, Regulatory, Legal, Market Access and Pharmacovigilance Ensure that any associated needs of health care professionals and other key customers in Italy are known, understood and addressed in right time and in a compliant manner Qualifications Advanced Medical or scientific degree (MD, PhD, PharmD) 10+ Years of relevant working experience in Medical Affairs within pharma/biotech Demonstrated leadership skills, with a successful track record in managing/coordinating field-based medical teams or medical science liaisons (MSL). Experience in Cardiology or related specialties and/or in rare cardiovascular diseases is advantageous Launch experience/expertise, ideally in specialty care is highly advantageous Strong understanding of the healthcare landscape, regulatory environment, and medical practices within Italy Excellent communication and presentation skills in both Italian and English, with the ability to effectively convey complex scientific information to diverse audiences. Proven expertise in KOL engagement, medical strategy, and collaboration with cross-functional teams. Proven ability to build strong relationships with KOLs and HCPs&nbsp; Ability to manage multiple priorities and manage time efficiently &nbsp;High ethical standards and familiarity with compliance guidelines in medical affairs Ability to work on their own, take initiative and accountability Strong ability to work remotely and adapt to a changing environment Ability to travel mostly national and if required in EU or globally Experience with Veeva or another CRM system#LI-REMOTE Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Associate Medical Director, Italy

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Cytokinetics is dedicated to upholding the highest standards of excellence to bring potential medicines to patients to improve outcomes and quality of life. We are looking for Regulatory Affairs professionals who bring a strategic mindset and a deep understanding of the regulatory environment. As a member of the team, you will play a crucial role in ensuring our processes meet regulatory requirements while maintaining high standards of compliance. Cytokinetics is seeking an experienced Director, Regulatory Affairs Europe to join the Regulatory Affairs team in Europe. He/she will provide leadership in developing and executing best in class regulatory strategies for assigned programs in the European region. The Director will lead regulatory activities related to the submission of Marketing Authorization Applications of assigned Cytokinetics products in Europe&nbsp; as well as implementation of post-marketing requirements. The Director, Regulatory Affairs Europe will work closely with the Global Regulatory Lead and be a member of the Global Regulatory Team. He/she will work cross-functionally including with Clinical Research, Medical Affairs, Drug Safety, Quality, Market Access and with country operations to ensure all regional and local regulatory requirements are met.&nbsp;&nbsp; The Director will also maintain awareness of the regulatory environment and communicate the impact of changes on business and product development programs. This position offers a temporary contract till end of the year, with possibility of extension. The work set up is hybrid, with 2-3 days per week in our centrally located Zug office, and the rest of the time from home. Responsibilities Develop a robust European strategy for specific products aligning with the Global regulatory strategy and cross functionally identify the best strategy that will lead to European approval. Contribute and independently execute the filing plans for Europe in line with corporate, regional and local business objectives. Ensure high-quality regulatory submissions are made on time and meet Cytokinetics requirements. Collaborate with the Regulatory Study Lead to review and provide strategic input/advice to EU CTR submissions and/or queries. As part of the Global Regulatory Team (GRT), provide direction and expertise on regional and local regulatory mechanisms to optimize product development Provide strategic and operational contributions to EMA/national agencies interactions and their preparation Maintain an awareness of new and developing legislation, regulatory policy and technical guidance relating to Cytokinetics products and discuss their implications with business. Oversees regulatory-related launch and post-marketing activities in the EU: Provides regulatory input to market access strategy and HTA plans and submissions in the EU Ensures all post-marketing requirements and maintenance activities are met. Work closely with the Quality department on relevant regulatory procedures applicable to the European region Qualifications Seasoned professional with a minimum of 10 years of relevant experience with a solid expertise and knowledge of the applicable European regulatory regulations, directives and guidelines. Bachelor of Science in a scientific discipline, Pharm D (/Pharmacist) or PhD preferred. Fluency in English, and any other key EU market languages are an advantage. Proven track record of directly leading Marketing Authorization Applications through EMA centralized procedure and national agencies (including Switzerland and UK).&nbsp;Experience in international markets is advantageous. Strong experience leading or participating in regulatory agency interactions. Solid foundation in science obtained through academics and business experience. Must be a strong team player, a fully engaged, hands-on professional capable of working collaboratively and independently, with excellent verbal and written communication skills. Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects. Strong interpersonal capabilities and ability to build and maintain networks. Possesses sense of urgency; identifies challenges and problems and takes the initiative to identify solutions. #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Director, Regulatory Affairs, Europe (contractor)

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Reporting to the General Manager Spain, the Commercial Director will lead all commercial activities in the region, including sales, marketing, and stakeholder engagement. They will drive launch readiness, build strong relationships with healthcare professionals, payers, and regulators, and shape Cytokinetics’ commercial strategy across the countries of responsibility. The role requires both strategic and operational leadership with deep Spanish healthcare knowledge, proven success in specialty product launches, and the ability to thrive in a fast-paced, entrepreneurial environment. As the company grows, the role will expand to include future product launches and broader commercial initiatives. As a senior leader, the role requires deep expertise in Italian healthcare systems, Regional Access dynamics, a proven track record in launching specialty therapies, and the ability to lead complex, multidimensional programs with significant corporate impact. Expertise on Cardiovascular market is a plus. The successful candidate will operate with a 1–3 year planning horizon, translating global strategy into regional execution, and influencing decisions that affect the long-term success in Spain. Key responsibilities:Strategic Leadership and cross-functional collaboration Develop and execute the Spanish commercial strategy for Cytokinetics assets. Implement Spanish commercial plans aligned with global and European objectives. Represent the commercial function on the Spanish Senior Leadership team. Monitor market dynamics and competitor activity to inform strategic decisions. Foster a culture of innovation, accountability, and patient-centricity, aligned to the Cytokinetics values. Work collaboratively across other functions to ensure customer needs are met. Sales team leadership Lead and manage the customer-facing field team to achieve regional sales targets. Recruit, develop, manage and retain a high-performing customer-facing commercial team. Establish performance standards, CRM systems KPIs and incentive schemes, driving a high performance culture by implementing minimum standards. Drive a high-performance culture through coaching, development, and operational excellence. Collaborate with market access to ensure alignment with payer and provider needs. External Cytokinetics ambassador with key centres/customers, supporting commercial uptake. Marketing Leadership Build and lead the Spanish marketing team, ensuring strategic alignment with global brand plans. Oversee development and execution of campaigns, congress strategies, and educational initiatives. Ensure compliance with regulatory standards and internal SOPs. Manage external vendors and agencies to deliver high-impact programs. Financial &amp; Operational Oversight, business planning Own the Spanish sales and marketing P&amp;L, delivering on revenue and profitability targets. Ensure operational excellence and compliance across all commercial activities. Lead the sales and marketing annual business planning process Set territory level budgets and forecasts aligned to country level aspirations Qualifications and experience Bachelor's degree in Life Sciences, Business, or related field; MBA or advanced degree preferred. 10+ years of commercial experience in the Spanish pharmaceutical or biotech industry, with proven success in launching and commercialising specialty or innovative therapies. Strong understanding of Spanish &amp; Portuguese healthcare systems, market access pathways, and regulatory frameworks. Exceptional leadership, communication, and stakeholder management skills. Ideally experience in cardiology or rare diseases Entrepreneurial mindset with the ability to thrive in a fast-paced, evolving environment. Strong analytical and strategic thinking capabilities. Proven ability to lead, inspire, and drive high-performing teams, with experience in matrixed and cross-functional collaboration Ideally experience in a small company environment #LI-HYBRIDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Commercial Director, Spain/Portugal

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Therapeutic Medical Scientist (Medical Science Liaison) Reporting to the Senior Medical Director for Italy, the TMS is a scientific professional who serves as a key field-based scientific resource for healthcare providers, patients, industry partners and internal colleagues. This role will come with high visibility in our company including critical cross-functional relationships across Medical Affairs, Clinical Development / Operations, and Commercial. This role will focus on key opinion leaders and other HCP’s in the hypertrophic cardiomyopathy therapeutic area, but also support pipeline products in development. Our passion is anchored in rigorous and diligent scientific and clinical approaches to the discovery and development of novel mechanism therapeutics. With gratitude for the commitments and convictions of our employees who are inspired by the courage of patients we aim to serve, we believe Cytokinetics will continue to be a pioneering, values-driven, sustainable, fully integrated biopharmaceutical company. Role and Responsibilities: Identify national, regional, and local Key Opinion Leaders (KOLs) involved in the provision of cardiovascular care within institutional care centres and engage them in proactive and reactive scientific exchange Maintain and enhance existing scientific collaboration and professional relationships with hospital-based HCPs within a defined geography (physicians, genetic counselors, hospital teams, investigators, etc..) involved in the therapeutic management of patients with cardiac diseases to expand research, advisory, and educational partnership opportunities; identify areas of unmet medical need; and assure thoughtful exchange of current medical information related to products in development and therapeutic areas of importance Serve as a scientific expert at key medical and scientific conferences, clinical investigator meetings, internal meetings, and patient advocacy group meetings Maintain a high-level of scientific knowledge and understanding about disease state, underlying science, treatment guidelines, available treatment agents and options, as well as other relevant therapies under development Maintain a superior understanding of current trends in clinical research, competitive developments, patient care, and their impact on Cytokinetics’ medical strategies Ensure prompt intake and responses for medical information, requests for Medical Affairs support and PV. Work with Medical Affairs and other internal colleagues on initiatives including medical information, publications, medical education, grants, speaker training, and other educational programs both within the country and internationally Generate Field Medical Affairs plans to identify collaborative opportunities with KOL’s and institutions, review scientific program of relevant conferences, attend sessions, support exhibit booth operations, and contribute to a timely written conference report summarizing key information, activities, and competitive intelligence to colleagues Provide support to our clinical development programs by serving as a key point of contact for company-sponsored trial investigators, investigator-initiated research, and registries consistent with company objectives and regulations Support and collaborate with the Local Sales Team in alignment with the Medical Plan and local requirements Contribute to build up the Account Planning by providing to the local Sales Team the required medical insights Provide initial and ongoing disease and product training to internal and field personnel. Identify congresses and scientific national and international meetings that are interesting and relevant to attend. Review scientific program of relevant conferences, attend sessions, support exhibit booth operations, and contribute to a timely written conference report summarizing key information, activities, and competitive intelligence to colleagues Accurate and timely documentation of activities within applicable company databases and platforms In addition to above, for Senior Therapeutic Medical Scientist: Mentor, train and support other Therapeutic Medical Scientists Provide scientific training on key relevant data to Key Account Managers and other business colleagues as required Provide strategic input and execute region-specific plans to achieve KOL engagement goals and Medical Affairs departmental goals Pursue projects independently with a high degree of quality and timely execution Contribute to / lead Congress Planning activities Maintain a complete awareness of and understanding about current “real world” clinical practices, HEOR drivers, and emerging trends in treatments/medicine Establish relationships with key executive leadership colleagues across Cytokinetics and connect external parties with appropriate leadership team members Qualifications Advanced clinical or scientific degree (BSc, MSc, BPharm, MPharm, PhD, BM BS or equivalent) preferred Minimum of 2-5 years of MSL experience for Snr. MSL. &nbsp;Experience in cardiovascular therapy area and / or hypertrophic cardiomyopathy is preferable. Experience in heart failure is beneficial but not required. Final position level will be determined based on overall experience Must be analytical and articulate in both oral and written communications, possess excellent presentation skills, with a demonstrated ability to communicate well with external stakeholders and all internal levels of the organization Must possess knowledge of the Medical Science Liaison roles and responsibilities and understand compliance within the ABPI Code Standards, AIFA and Farmaindustria rules &amp; regulations for Interactions with Italian Healthcare Providers and all other company policies, rules and regulations Comply with all credentialing requirements for any healthcare institution which is part of the Medical Science plan, including, among other things, routine background checks, medical testing or proof of immunisations, training on facility policies, and adherence to confidentiality and/or other agreements Proficiency with Microsoft Office and web-based applications A valid Driver’s License and good driving record are required Ability to travel both domestically (~30%-50%) and internationally on occasion (TBD)#LI-HYBRID Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Therapeutic Medical Scientist, Italy

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Job purpose The role will provide structured assistance across document management, complaints handling, reporting, and general administrative activities. Securing this support will improve operational efficiency, strengthen compliance, and enable QA professionals to focus on high-value quality and oversight responsibilities. The Quality Department operates in a highly regulated environment with increasing demands related to documentation, customer assurance, and quality reporting. QA administrative workload has grown significantly, particularly in areas such as complaints management, CMO scorecard development, and compliance checks. Responsibilities The Quality Associate support will initially provide approximately 20 hours per week of support across the following key areas Document Creation and Execution Support Preparation, formatting, and maintenance of QA documentation within Veeva Coordination of document lifecycle activities including review and version control Ensuring adherence to internal documentation standards Complaints Management Support Initiating and tracking of customer complaints Supporting data entry, documentation, and follow-up activities Assisting in maintaining audit-ready complaint records CMO Scorecard Development Supporting data collection and consolidation for CMO performance metrics Assisting in the preparation and formatting of scorecards and reports Maintaining consistency and accuracy in reporting outputs Distribution and Quality Disposition Support Coordinating distribution of quality-related documents and communications e.g. disposition returns Supporting quality disposition processes and maintaining executed record logs e.g Temperature excursions Facilitating communication between internal and external stakeholders as needed Bona Fide Customer Checks Conducting verification checks on customers Maintaining accurate and traceable records of compliance activities Supporting QA in meeting regulatory and internal compliance requirements General Administrative Support (Ad Hoc) Event and meeting organization Additional administrative duties as required Qualifications Required Qualifications Bachelor’s degree in Life Sciences, Biotechnology, Chemistry, Engineering, or a related scientific discipline Approximately 5 years of hands-on experience in a life sciences Quality environment (biotech, pharmaceutical, medical device, or regulated healthcare industry) Demonstrated experience supporting Quality Assurance (QA) and Quality Management System (QMS) activities Strong working knowledge of GxP requirements (e.g., GMP, GDP) and regulated documentation practices Proven experience with document creation, formatting, execution, and lifecycle management within an electronic document management system (e.g., Veeva Vault or similar) Experience supporting complaints management processes, including documentation, tracking, and maintenance of audit-ready records High attention to detail with the ability to maintain accurate, compliant, and traceable records Strong organizational and time management skills, with the ability to manage multiple tasks and prioritize effectively in a part-time (approximately 20 hours/week) support role Excellent written and verbal communication skills, with the ability to interact professionally with internal and external stakeholders Proficiency with Microsoft Office tools (Word, Excel, PowerPoint), particularly for data consolidation, tracking, and reporting#LI-HYBRID Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Associate Director, Commercial Learning & Development

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