Nuvalent is a biopharmaceutical company dedicated to developing targeted therapies for patients with cancer.

The Company:With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&nbsp;The Role:Reporting to the Senior Medical Director, Pharmacovigilance, the Associate Director, Drug Safety and Pharmacovigilance Scientist is responsible for assessing and interpreting safety data from multiple sources, including clinical trials, spontaneous and solicited reports, aggregate, and literature reports. This individual is expected to provide interpretation and summaries of drug safety information and provide input in the generation of safety reports (e.g., DSURs, PSUR and clinical safety assessments). The individual will be an integral part of a group of safety professionals within Nuvalent and will closely collaborate with safety teams in Contract Research Organizations (CROs) and partners. He/she will need to maintain medical knowledge as required by the role, strong and current knowledge of drug safety and pharmacovigilance regulations, pharmacovigilance practices, safety surveillance and risk-management practices. Responsibilities:• &nbsp; &nbsp;Provide medical expertise in the assessment of ICSRs&nbsp;• &nbsp; &nbsp;Contribute to the generation of aggregate safety reports including development safety update reports, periodic benefit risk evaluation reports, and provide medical input in review of new or existing safety documents to ensure compliance with relevant regulatory requirements, such as protocols, safety summaries and regulatory reports• &nbsp; &nbsp;Contribute to signaling and safety surveillance process, including the identification of safety observations, emergent safety concerns and new safety signals, ensure prompt assessment and communication of confirmed safety signals• &nbsp; &nbsp;Serve as a medical resource for the generation and review clinical trial protocols, informed consent forms (ICFs) and investigator brochures (IBs) and the development of Reference Safety Information• &nbsp; &nbsp;Contribute to creation or and updates to Risk Management Plans (RMPs) and/or Risk Evaluation and Mitigation Strategies (REMS) and the maintenance of these documents• &nbsp; &nbsp;Contribute to the development of Standard Operating Procedures, Working Instructions and other guidance documents• &nbsp; &nbsp;Provide safety and pharmacovigilance training programs as required• &nbsp; &nbsp;Collaborate cross functionally (e.g. Reg Affairs, Clin Ops, Clin Science) to ensure pharmacovigilance input• &nbsp; &nbsp;Support other pharmacovigilance and drug safety responsibilities as assigned&nbsp;Competencies Include:• &nbsp; &nbsp;Strong written/verbal communication skills.&nbsp;• &nbsp; &nbsp;Ability to work in a collaborative environment and build effective working relationships across the organization, and with external stakeholders/vendors• &nbsp; &nbsp;Detail and process orientated, with excellent project management, problem solving, and organization skills.• &nbsp; &nbsp;Ability to think critically with strong attention to detail.• &nbsp; &nbsp;Demonstrated project management and prioritization capabilities Qualifications:&nbsp;• &nbsp; &nbsp;4+ years’ experience in Drug Safety / Pharmacovigilance in a pharmaceutical or biotech company, CRO or regulatory agency• &nbsp; &nbsp;Healthcare degree required / Medical Degree (MD) from recognized medical school preferred.&nbsp;• &nbsp; &nbsp;Good working knowledge of US and EU drug safety regulations, CIOMS and ICH guidelines• &nbsp; &nbsp;Demonstrated experience with medical drug safety assessments, drug safety surveillance and monitoring activities• &nbsp; &nbsp;Proficiency with medical review of ICSRs, including expectedness assessments, causality assessments, narrative review and generation, generation of Analysis of Similar Event and company comment statements, including benefit-risk assessment.• &nbsp; &nbsp;Experience with safety data collection and interpretation originating from clinical trials and other sources (such as literature, solicited and post-marketing environment)• &nbsp; &nbsp;Experience with the medical review and preparation of aggregate reports (DSUR, PSUR/PBRER, PADER)• &nbsp; &nbsp;Experience with preparation of responses to Regulatory Authorities, preferred experience with IND/NDA submissions and negotiations with Regulatory Authorities as part of marketing approval• &nbsp; &nbsp;Experience with the development and updates to Reference Safety Information, including IB, Company Core Data Sheet (CCDS) and local labels• &nbsp; &nbsp;Ability to build relationships, collaborate and influence across disciplines within Nuvalent and with outside stakeholders• &nbsp; &nbsp;Experience with MedDRA coding, Points to Consider, AoSE, and SMQs• &nbsp; &nbsp;Excellent verbal, written and presentation skills &nbsp;Nuvalent&nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities. Please be advised that all legitimate correspondence from a Nuvalent employee will come from "@nuvalent.com" email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “no-reply@greenhouse.io” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.

Associate Director, Drug Safety and Pharmacovigilance (PV) Scientist

The Company:With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&nbsp;The Role: Reporting to the Deputy General Counsel, Commercial and Compliance, the Senior Counsel, Product will be a critical part of Nuvalent’s Legal Department and will contribute significantly to the success of our growing organization. In this role, you will be responsible for advisement on a host of strategic and tactical issues related to the development and future commercialization of prescription drug products. Responsibilities will include advising on matters governed by healthcare fraud and abuse laws, FDA regulations, state and federal drug pricing and transparency laws, access and reimbursement matters, privacy laws and providing legal guidance on patient support programs. The Senior Counsel, Product will act as the brand lawyer and reviewer on the Promotional Materials Review Committee and the Medical Review Committee. This role will also support cross functional compliance initiatives and other key projects across the organization. We are looking for an attorney with product launch experience, a proactive mindset and solution orientation to join the Nuvalent team. &nbsp; Responsibilities: Serve as a legal advisor on a broad range of commercialization-related subjects in support of anticipated launch of company’s first oncology product to the cross functional brand team, including marketing, medical affairs, market access, sales, and other key stakeholders. Serve as an experienced subject matter expert and review committee member for advertising, promotional and non-promotional materials, and medical materials, including sales and marketing materials, market access materials, patient support program information, disease education, scientific exchange, press releases, and clinical trial recruitment activities. Serve as a legal business partner to market access team Provide legal advisement on the design and implementation of sales and marketing strategy, market access activities, patient support programs, medical affairs initiatives, media campaigns, and interactions with patients and patient advocacy organizations. Provide ad-hoc advice on contracts with health care fraud and abuse, FDA or brand related implications. Advise on commercialization-related contracts and engagements, including distribution agreements, GPO agreements, rebate agreements, specialty pharmacy agreements, vendor agreements, service agreements, consulting agreements, and sponsorships. Serve as a legal representative on cross functional project teams, as assigned, to support business initiatives, identify and mitigate legal risks and to foster collaboration across other legal and compliance disciplines as appropriate. Assist in the development of the enterprise-wide compliance program Additional responsibilities as assigned Competencies include: Experience as the legal representative on a promotional review committee and a medical materials review committee in the pharmaceutical industry Experience in advising on healthcare fraud and abuse laws Experience advising on matters governed by FDA regulations Experience advising on patient support programs and market access initiatives Ability to provide responsive, thoughtful, pragmatic and clear advice in support of business objectives Clear communication style that effectively conveys advice and recommendations to key stakeholders A demonstrated track record of acting with integrity and a collegial, solution-oriented mindset A champion of a positive and respectful company culture Qualifications: 7+ years of recent relevant legal experience in product support of biotech/pharma, with a strong preference for experience with launching a product in the U.S. market and 3+ years in-house pharmaceutical or biotech oncology experience Juris Doctor from an accredited law school; active membership and in good standing in a state bar and either admitted to the Massachusetts bar or eligible for admission to the Massachusetts bar as in-house counsel Significant knowledge of enforcement trends, the Federal Food, Drug and Cosmetic Act and related regulations, the False Claims Act, and laws related to fraud and abuse in the life science/biotech/pharma industries&nbsp; Experience with pharmaceutical/biotech commercial contracting preferred Team player with strong and effective collaboration and communication skills Ability to travel as required to support business activities. Nuvalent&nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities. Please be advised that all legitimate correspondence from a Nuvalent employee will come from "@nuvalent.com" email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “no-reply@greenhouse.io” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.

Senior Counsel, Product

The Company:With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&nbsp;The Role: Reporting to the Vice President, Biostatistics, the Senior Biostatistics will serve as the project lead statistician responsible for statistical activities at study level and compound level, including, protocol development, study design, statistical data analysis, regulatory submissions, publications, and presentations at Nuvalent. The Senior Director, Statistics will also oversee CRO statistics deliverables for all Nuvalent studies. Responsibilities: Lead the development of statistical sections of clinical study protocols, statistical analysis plans, and conduct the analysis and reporting of clinical trial data Provide strategic input to optimize trial designs in early phase dose escalation studies and late phase registrational studies Oversee CRO statistical activities and manage contractor statisticians to ensure timely delivery of high-quality statistical outputs As the biostatistics representative, proactively collaborate with internal and external team members in the assigned projects, accountable for all statistics deliverables Contribute to the biostatistics vendor evaluation and selection Provide a thorough review for required components of regulatory submissions including appropriate datasets, define files, reviewer's guides, and other relevant documents Contribute to the development of Biostatistics SOPs and standards Support study/program-level audit and inspection readiness activities as needed Develop and maintain advanced competencies in statistical methodology and advanced trials designs, particularly in oncology drug development Competencies: Adaptability/Flexibility – The ability to adapt to working effectively within a variety of situations; adapts enthusiastically to organizational change and to changes in job demands. Communication and Teamwork – Ability to effectively express ideas in written and oral context; to work co-operatively with others; genuine desire to be a part of a team and contribute to organizational and team goals. Effective Planning – Embed discipline and thoroughness in our approaches. Perseverance – Pursues tasks with energy, drive, and initiative, even in the face of adversity; comfortable in a results-driven, highly accountable environment where you can make an impact. Problem Solving – Ability to understand a situation or problem by breaking it down into smaller pieces using a systematic approach and to identify patterns and connections between situations that are not obviously related. Relationship Building – Builds productive working relationships across a diverse spectrum of people. Organizational Skills – Ability to handle multiple responsibilities simultaneously and still meet high quality and timeliness standards under pressure. &nbsp;Qualifications: Minimum of MS required (Ph.D. preferred) in Statistics, Biostatistics, or other related fields MS with 12+ years (Ph.D. with 8+ years) of overall experience, including at least 10+ years (at least 6+ years for Ph.D.) of experience in drug development in a CRO or pharma/biotech company Oncology experience is strongly preferred: familiar with oncology drug development, both early and late stage, including efficacy endpoints, RECIST criteria, common statistical issues and study designs in oncology Regulatory NDA/BLA submission experience is strongly preferred Must have hands on experiences with SAS programming in clinical studies Experience with managing CROs and contractors Excitement about the vision and mission of Nuvalent and working on drug development Excellent project management skills and proven ability to manage competing priorities Nuvalent&nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities. Please be advised that all legitimate correspondence from a Nuvalent employee will come from "@nuvalent.com" email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “no-reply@greenhouse.io” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.

Senior Director, Biostatistics - Oncology

The Company:With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&nbsp;The Role:Reporting to the Vice President, Clinical Development, the Senior Medical Director, Clinical Development provides an excellent opportunity for a physician with experience in oncology clinical development to work within a rapidly growing company. The Senior Medical Director, Clinical Development is responsible for providing medical leadership, medical monitoring, and executional oversight of clinical studies, and to pave a path towards regulatory approval. The Nuvalent pipeline is currently focused on development of precision medicines for oncology targets; therefore, the physician will work closely with a multi-disciplinary team consisting of non-clinical safety, DMPK/clinical pharmacology, biostatistics, clinical operations, data management, pharmacovigilance, and regulatory affairs. &nbsp;The physician will also lead and participate in teleconferences with academic study investigators, safety review committees, advisory meetings with opinion leaders, and interactions with Health Authorities. This position will report to the Vice President of Clinical Development. Responsibilities:• &nbsp; &nbsp;Hands-on involvement in clinical studies that will support regulatory approvals• &nbsp; &nbsp;Be the clinical lead for clinical trials, including performing detailed review and evaluation of molecular pathology reports for eligibility, and ongoing monitoring of clinical and laboratory data, assessing safety, and responsibility for analysis of emerging safety and clinical signals.• &nbsp; &nbsp;Provide clinical expertise and writing of clinical sections of key documents, including Investigator’s Brochures, IND summary documents, CTAs for initiation of studies ex-US, responses to questions from regulatory authorities, IRBs and ethics committees, and NDAs• &nbsp; &nbsp;Leading investigator meetings and networking opportunities with academic clinical investigators• &nbsp; &nbsp;Attending and supporting clinical site initiation visits&nbsp;• &nbsp; &nbsp;Provide medical review, assessment and interpretation of all clinical data reported in clinical study reports to ensure that the data are correct and presented with the appropriate medical interpretation• &nbsp; &nbsp;Work closely with Regulatory Affairs, and multi-disciplinary team to assure timely filing of all regulatory documents and applications• &nbsp; &nbsp;Provide Pharmacovigilance support for the clinical trials in conjunction with our PV team• &nbsp; &nbsp;Ensure consistent practices with the highest ethical standards in compliance with internal SOPs, local regulations and laws• &nbsp; &nbsp;Serve as the clinical face of the company both internally and externally, including the scientific community and key opinion leaders• &nbsp; &nbsp;Support study/program-level audit and inspection readiness activities as needed&nbsp;Competencies Include:• &nbsp; &nbsp;Excellent interpersonal and communication skills with ability to build positive, effective relationships with both internal and external stakeholders• &nbsp; &nbsp;Ability to work productively primarily from home in a fast-paced, results-driven, highly accountable environment where you can demonstrate initiative and make a clear impact Qualifications:&nbsp;• &nbsp; &nbsp;An M.D. or M.D/Ph.D. with experience in oncology is required (subspeciality training in oncology and experience in targeted therapy lung cancer trials preferred)• &nbsp; &nbsp;4+ years of proven ability in the biotechnology or pharmaceutical industry including direct experience leading high functioning teams• &nbsp; &nbsp;Thorough understanding of the drug development process from IND through NDA, including novel clinical study designs, application of companion diagnostics for patient selection, clinical operations and pharmacovigilance• &nbsp; &nbsp;Experience in clinical research, including designing, planning and monitoring clinical trials.• &nbsp; &nbsp;Experience with high-complexity first-in-human studies is highly desired• &nbsp; &nbsp;Experience presenting to a variety of audiences including internal teams and external medical/scientific communities• &nbsp; &nbsp;Experience with interacting with Regulatory Authorities, such as FDA and EMA is preferred.• &nbsp; &nbsp;Ability to travel domestically and internationally to investigator sites and medical meetings, approximately 10%Nuvalent&nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities. Please be advised that all legitimate correspondence from a Nuvalent employee will come from "@nuvalent.com" email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “no-reply@greenhouse.io” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.

Senior Medical Director, Clinical Development (MD Required)

The Company:With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&nbsp;The Role: Reporting to the Senior Director, Commercial Insights and Analytics, the Director, Commercial Forecasting and Analytics will be responsible for leading market research, forecasting and additional commercial insights and analytics initiatives in support of key business decisions across the NSCLC portfolio. This role will provide deep understanding of current market trends, competitive intelligence, and customer perspectives to drive commercial strategy, product positioning, and launch readiness. The ideal candidate is an experienced market research, forecasting, analytics and/or commercial insights professional with a strong background in oncology, particularly NSCLC, and a passion for using data-driven insights to guide business strategy. &nbsp; Responsibilities: Develop and lead the market research and analytics strategy to support pre-launch planning, brand forecasting/long-range planning, future marketed products, and pipeline assets. Define and oversee high-level strategic initiatives in market intelligence, competitive landscape analysis, and commercial insights generation in collaboration with Corporate Strategy team. Serve as a strategic advisor to leadership, proactively identifying opportunities and risks within the NSCLC market that help shape brand strategies. Lead the development of commercial forecasting models in support of near-term execution and longer-term business strategy development. Partner cross-functionally with Commercial, Medical Affairs, Market Access, Supply Chain, and Clinical Development teams to ensure research findings align with business objectives and can be translated into compelling, actionable recommendations for the Nuvalent executive leadership team. Establish key performance indicators (KPIs) and reporting frameworks to monitor market trends, launch performance, and commercial effectiveness. Work with I&amp;A peers to lead qualitative and quantitative research and analytics (including ad-hoc) to understand physician, patient, and payer perspectives on NSCLC treatment landscapes. Lead ongoing competitive landscape assessments, monitoring key players, clinical developments, and emerging trends in NSCLC. Identify key market trends, unmet needs, and opportunities to shape brand strategy and commercialization efforts. Drive the integration of advanced analytics, artificial intelligence models, and machine learning into business intelligence and commercial planning. Mentor broader Commercial Insights &amp; Analytics team members, fostering a culture of strategic thinking, innovation, and professional development. Manage relationships with third-party vendors and external market research partners, ensuring high-quality, actionable insights. Represent the organization at industry conferences, investor presentations, and high-level strategic discussions as required. Competencies Include: Foster a culture of empowerment, collaboration, and a focus on patient impact. Strategic Thinking – Ability to translate complex data into meaningful business insights and influence commercial strategy. Leadership &amp; Communication Competencies Executive Presence &amp; Influence – Ability to present insights persuasively to senior leadership and cross-functional teams. Cross-Functional Collaboration – Strong partnership skills with Commercial, Medical Affairs, Market Access, and Clinical Development teams. Problem-Solving &amp; Decision-Making – Aptitude for identifying challenges and providing data-driven recommendations. Communication &amp; Storytelling – Ability to distill complex primary and secondary research findings and analytical output into compelling narratives for diverse audiences. &nbsp; Qualifications: Bachelor’s degree in Business, Life Sciences, or a related field (MBA or advanced degree preferred). 10+ years of forecasting and analytics experience, with at least 5 years in oncology (NSCLC preferred). Proven expertise in qualitative and quantitative research methodologies, competitive intelligence, and data analytics – specifically to support forecast development (e.g. demand studies, chart audits, EMR data synthesis, etc.) Strong understanding of NSCLC treatment paradigms, KOL perspectives, and market dynamics. Experience supporting product launches and commercial strategy development. Ability to synthesize complex data into clear, impactful insights for senior leadership. Strong vendor management skills and ability to drive projects within budget and timelines. Excellent communication, presentation, and strategic thinking skills. Experience building systems, processes, and support structures within fast-paced, start-up environments preferred. Nuvalent&nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities. Please be advised that all legitimate correspondence from a Nuvalent employee will come from "@nuvalent.com" email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “no-reply@greenhouse.io” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.

Director, Commercial Forecasting and Analytics

The Company:With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&nbsp;The Role: Reporting to the Vice President, Marketing, the Director, Market Access Marketing plays an essential role executing the Market Access and Pricing strategy to ensure zidesamtinib and neladalkib are strategically positioned for payer access, organized customer coverage, and patient access. This role will be responsible for payer marketing, organized customer marketing, reimbursement strategy, and market access initiatives to optimize coverage, adoption, and reimbursement. Given the cross-functional nature of the role, the market access marketer will have a dotted reporting line to the Senior Director, Payer and Reimbursement. S/he will also collaborate closely with Sales, HEOR, and Medical Affairs to drive launch readiness and post-launch success. Responsibilities: Strategic Planning Payer &amp; Health Care Decision Maker (HCDM) Messaging Strategy – Develop compelling value propositions and messaging highlighting clinical benefits, cost-effectiveness and differentiation. Agency Selection – Manage market access marketing AOR to refine strategy, messaging, and materials. Work with cross-functional teams to develop pricing, reimbursement, and contracting strategies aligned with business objectives. Identify and capitalize on strategic opportunities to best position Nuvalent products in National Accounts (e.g., National GPOs, Aggregators, Physician Networks, Pathways and Strategic Partners), including and beyond annual meetings, conferences, congresses which this role will oversee &nbsp; Market Access &amp; Payer Engagement Support Develop Market Access Materials – Create tailored presentations, digital content and key messaging for payers and providers Pre-Approval Information Exchange (PIE) – Refine and implement PIE strategy, messaging and materials to meet payer expectations and regulatory guidelines. Value Proposition – Craft evidence-based messaging to support formulary inclusion, reimbursement pathways and EHR integration. FAQs &amp; Reimbursement Guide – Prepare pricing, coding and coverage documents addressing payer concerns. Distribution Selling Sheets – Equip distribution partners with materials on product availability and logistics. &nbsp;Integrated Delivery Network, GPO Engagement, &amp; Patient Services Support Access Materials for IDN, GPO HCDMs – Educate healthcare professionals on reimbursement and formulary details. Patient Support Programs – Develop resources for PSP including financial assistance and copay support. Patient Access Content – Ensure patients have clear coverage, affordability, and access guidance. Hub Forms – Design enrollment and specialty pharmacy documentation. &nbsp;Internal Training &amp; Strategic Insights Training Materials for Sales – Provide customized access and reimbursement guides for sales team External Access Communications – Updating external stakeholders on formulary status and changes Industry Education – Develop educational content on IRA Medicare Part D Benefit Redesign and Medicare Part C/D background. Stakeholder Insights – Organize Payer &amp; Provider Advisory Boards for market insights. Competitive &amp; HEOR Analysis – Incorporate relevant HEOR into value messaging and monitor pricing, access strategies and cost-effectiveness data to incorporate. Regulatory &amp; Compliance Oversight – Ensure all materials meet FDA, CMS, and payer regulations. &nbsp;Competencies Include: Entrepreneurial spirit and disruptive mindset. Successful track record working in a fast-paced, rapid-growth environment. Excellent interpersonal skills, with the ability to gain alignment by working collaboratively and inclusively across functional teams. Strong verbal and written communications. Proven ability to grow and develop others. Record of achievement, innovation, and compliance. Qualifications: Bachelor’s degree required; advanced degree (MBA, PharmD, or PhD) preferred. 10+ years of experience in biotechnology, pharmaceuticals, or healthcare with a focus on market access, payer marketing, or reimbursement strategy. Product launch experience, preferably including oral products in oncology Experience collaborating with NCCN for development of bespoke NPP and personal promotion materials for providers Deep understanding of payer and reimbursement landscape, including Medicare, Medicaid, and commercial insurers. Experience developing and executing market access strategies in a commercial launch setting. Strong analytical skills and ability to translate data into actionable insights. Excellent cross-functional collaboration and communication skills. Ability to manage multiple projects and drive results in a fast-paced environment. &nbsp;Nuvalent&nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities. Please be advised that all legitimate correspondence from a Nuvalent employee will come from "@nuvalent.com" email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “no-reply@greenhouse.io” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.

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