Kura Oncology is a biopharmaceutical company dedicated to discovering and developing innovative cancer therapies. Through cutting-edge research and a focus on precision medicine, Kura Oncology aims to revolutionize cancer treatment and improve patient outcomes.

kura-oncology

<div class="content-intro">Are you ready to join a team committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines? At Kura Oncology, you have an opportunity to be a part of something bigger, with a lasting impact that you can be proud of.
At Kura Oncology, we are working to change the paradigm and improve the science of cancer treatment. As an organization, we strive to cultivate a diverse and talented professional culture driven to develop precision medicine therapeutics.
As we continue to build a leading biotech organization with a strong culture, a patient-focused mindset and a team focused on relentless execution, we are looking for innovative, passionate professionals to join us and make our vision a reality.
To succeed at Kura, you will need to have a demonstrated ability for excellence in drug discovery and development and a roll-up your sleeves attitude. The ideal candidate will possess a values-driven work style where integrity and grit drive all behaviors, decisions, and actions.</div>ESSENTIAL JOB FUNCTIONS:
The Director, Clinical Business Operations is responsible for leading strategic and operational initiatives that enable the efficient execution Clinical Operations activities. This role serves as a key business partner across Clinical Trial Management, Clinical Data Sciences, Clinical Systems, Biosample Operations, and other cross-functional team members to drive operational excellence, portfolio visibility, resource planning, performance measurement, and process optimization.
The Director will establish and maintain business processes, operational metrics, governance frameworks, and reporting capabilities that support informed decision-making and execution of the clinical portfolio. This individual will work closely with Clinical Operations leadership to identify risks, improve organizational effectiveness, and ensure alignment between strategic objectives and operational execution. Clinical Operations Leads remain accountable for program strategy and operational execution while Clinical Business Operations provides department-wide planning, governance, reporting, systems, and business infrastructure.
This is an exciting opportunity for a seasoned Clinical Operations leader who has mastered clinical study management and wants to make the leap to a clinical business excellence role.
Strategic Planning &amp; Governance
<ul>
<li>Support annual and long-range strategic planning activities for the Clinical Operations organization.</li>
<li>Coordinate portfolio governance processes and facilitate leadership review meetings.</li>
<li>Develop and maintain business operating rhythms, including leadership team meetings, performance reviews, and planning cycles.</li>
<li>Drive cross-functional initiatives aligned with departmental and corporate objectives.</li>
</ul>
Operational Excellence
<ul>
<li>Lead continuous improvement initiatives focused on quality, efficiency, scalability, and execution excellence.</li>
<li>Develop and implement standardized business processes across Clinical Operations functions.</li>
<li>Identify operational bottlenecks and recommend solutions to improve performance and organizational effectiveness.</li>
<li>Partner with stakeholders to ensure successful implementation of process and organizational changes.</li>
</ul>
Metrics &amp; Performance Management
<ul>
<li>Establish and maintain key performance indicators (KPIs) and operational dashboards.</li>
<li>Deliver meaningful portfolio and departmental performance reporting to leadership.</li>
<li>Analyze trends and identify opportunities to improve study execution, organizational performance, and resource utilization.</li>
<li>Support development of executive-level presentations and business reviews.</li>
</ul>
Resource Planning &amp; Financial Oversight
<ul>
<li>Coordinate resource forecasting and capacity planning activities across Clinical Operations functions.</li>
<li>Partner with Clinical Operations Leads, Finance and functional leaders to support budget planning and tracking.</li>
</ul>
Systems &amp; Business Enablement
<ul>
<li>Provide functional business ownership for systems spanning multiple functions (e.g., eTMF and CTMS) and partner with Clinical Systems and Technology teams to optimize tools, platforms, and business processes.</li>
<li>Drive adoption of systems and technologies that enhance operational effectiveness.</li>
<li>Ensure data integrity and consistency across operational platforms.</li>
</ul>
Leadership
<ul>
<li>Manage and develop clinical trial associates and business operations staff as applicable.</li>
<li>Foster a culture of accountability, collaboration, innovation, and continuous improvement.</li>
<li>Influence cross-functional teams without direct authority to achieve organizational goals.</li>
<li>Complete other duties as assigned by the manager</li>
</ul>
JOB SPECIFICATIONS:
<ul>
<li>Bachelor’s degree in science/healthcare field, a nursing degree, or equivalent combined education.</li>
<li>A minimum of 10-12 years of strong hands-on experience leading large, complex Phase 3 clinical trials preferably in oncology/hematology in US, Asia, Europe; or equivalent combination of training and experience.</li>
<li>Proven ability to build strong relationships with external partners, CROs, and vendors including extensive experience managing clinical operations activities.</li>
<li>Foundational skills in financial and resource planning, and business management acumen.</li>
<li>Ability to work independently and collaboratively in a fast-paced, matrixed, team environment consisting of internal and external team members.</li>
<li>Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines.</li>
<li>Excellent communication and presentation skills.</li>
<li>Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects.</li>
<li>In-depth, working knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.</li>
<li>Flexibility to travel domestically and internationally as required.</li>
<li>Owns decision-making for their functional area or program, including resolving complex issues and making trade-offs to achieve program objectives, with minimal escalation.</li>
<li>Leads cross-functional collaboration for assigned programs, proactively driving alignment across stakeholders and resolving issues to support program execution.</li>
</ul>
The base range for this role is $231,000 - $264,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location, and relevant education or training. Kura's compensation package also includes generous benefits, equity, and participation in an annual target bonus.
#LI-RM1<div class="content-conclusion">Kura’s Values that are used for candidate selection and performance assessments:
<ul>
<li>We work as one for patients</li>
<li>We are goal-focused and deliver with excellence</li>
<li>We are science-driven courageous innovators</li>
<li>We strive to bring out the best in each other and ourselves</li>
</ul>
The Kura Package 
<ul>
<li>Career advancement/ development opportunities</li>
<li>Competitive comp package</li>
<li>Bonus</li>
<li>401K + Employer contributions</li>
<li>Generous stock options</li>
<li>ESPP Plan</li>
<li>20 days of PTO to start</li>
<li>18 Holidays&nbsp; (Including Summer &amp; Winter Break)</li>
<li>Generous Benefits Package with a variety of plans available with a substantial employer match</li>
<li>Paid Paternity/Maternity Leave</li>
<li>In-Office Catered lunches</li>
<li>Home Office Setup</li>
<li>Lifestyle Spending Stipend</li>
<li>Commuter Stipend (Boston Office)</li>
<li>Regular employee social activities, including happy hours, monthly birthday celebrations, Kura Koffee Talks, and much more!</li>
</ul>
Kura Oncology is a commercial-stage biopharmaceutical company committed to discovering and developing innovative precision medicines to help patients with cancer lead better, longer lives.
Through our deep understanding of cancer biology and decades of experience in precision oncology, we are studying the underlying causes of treatment resistance. This enables us to design smart combination regimens with other cancer therapies to target tumors from multiple directions, with the goal of improving long-term clinical benefit.
Kura developed and is commercializing KOMZIFTI® (ziftomenib), the FDA-approved once-daily, oral menin inhibitor for the treatment of adults with relapsed or refractory NPM1-mutated acute myeloid leukemia, and continues to pioneer advancements in menin inhibition and farnesyl transferase inhibition. For additional information, please visit Kura’s website at&nbsp;<a href="https://www.globenewswire.com/Tracker?data=ivPIaZ1M97sI-f2KN-08EdPH6mjSpiSN5KlK5_wlQbAAc4LWQocEKA9WUvb12WpwAN9k7iI4dL7FhQDxff_oY9qsBJJggCsRDLKBn9d-juCsq_E1nYXWUbPkipiFX7v6c5txgiRkYTmedLH_CMbGZGrwjGeppu4zTKTte98OnPG6O31YTGLfYCMEgU_q7Nda9e_0jwSblQw2MaRpdEflJOyNutWjOqPotKN5lxqDg-Y1UUF9H972qTWMlpwJdASFnH4jOkFTx4G1ePOUVApIr4lh_Q4tBul_A5aN9Go-704pV8GyzBO3XsQh6R2zmyotgeo7OJSsVJWiPMbdy8Xdpk0xIB81zv7DL1skxttlNuoVFX2_gQqD22FlIZX0eJTHeJ4_Im5HsRBZxO8iY08JPj9YO5W8wQjQbQGCEeCWAtJOzt79X-w9kpWvV30q2_Nv3_GHClF6m_ipTs6A3Dni9l8ihAggbB8JCtlahmKisZOERjyUz15eR5cyoeIbeX34hCzjvnsVJq2WYbfXyUWRcQ==">www.kuraoncology.com</a>&nbsp;and follow us on&nbsp;<a href="https://www.globenewswire.com/Tracker?data=0XrzPmD93VFEFgLaVr3RDXJ4YJ9GwVIrdBdEpaZqOXlWVFt2wNf-GaUGGD7vAJGfpHH18a0knFqQZ3VKcNbSrfyAweMLIwpkC8zrSNvFkBKLuOr_mnRS1Dq1TXP3--WW3ozJKzm5Tf2uvnAeJde-MlQBsDQieWSjNaw9g8uMPbWUxqjjWPc-YvQO5FjwEFspnPDZ7SsZ9Tj6xZxHPbhm0cG1woV_LAfBhUuAUorGYEwe1p023CEmpdHBqytB1Hb2Lca3QvrupWDzdPliVnBnazwblrZopi5a9BjP35irdevpYuevM0xDkPqhUbDaUOzsO8quAx--cMtliGWkIqyNO8BBXruqdidcb-dKXVzK9nnWNdBqNyJdnGJ_FKMNtSgvxpSjFm89EWwQk-2tCFVy-c3DiP3QOTNUsNZfdDvdalWiXA790TBE8-m6he3SH5kJE0jHosqjsWdQZ_LmmhF-APnsj5zLK30H9lJT_96t4y7taBZS9EgCbnKlIuMtg4Xt5QZ3XfY4a4QFzsKkZGcGZaOxBs148YXiBRrEMpHuVxm9Ed81NLoog4lyhe73Qdj3GJgvxI_UpHE9P2EWjVIO8wztEdDxd5kzg8Rbdp-HQ6fVkffcVZUaw1aYoJbRztrn9uzPu0qhXXcEooOlLAVcfA==">X</a>&nbsp;and&nbsp;<a href="https://www.globenewswire.com/Tracker?data=09ovKsXTlPV0n7MjNVrrRqAWBywJUeOxMzA_nYB0Mk0aAGczYB85764GV7bV1rte53dGawh5WyBhpHnXGI3ssuWm-1o-T3NalGIRz42ZpjYzyMPck9PFykD3kxqzRwUW5X1cNHoiCrfr5XfhWSBbdOWzC0i3dmxbxaPyBaKvqdJJIoR5mFg0YjYqYom9B-2uixJr1C2ZRKFqzkhKjPfkfPRiHu0QgJbQ8VPufnQc5Ac_860SJQLIG4kctJSyc1w4Ffp5NzgO0puLINW3Xsssd8lishssXKnQRc6IqzmMb3u1-FAJBoOauwh-pIEfxweaJy1Es3TEUOcN1aC0PFe8Cjp3IAkNSMq-1imazyxbc7QP4xj93QysOCLUdwT62O3Y4nP3TSl5cHBn2DIiUxW70gqQ04L2wUWgy14Tpl5CEYJ_Hp_JG3JIwh0SCWhbF7uPWoXfbcrK-jMjSsVM8JoNm7pt5tWA5e5m5iIFpNFP-Gn0zx9jrc3TinLD9ksPonmmf6uEP1loaxtKd5rIPeTu69E9mgnOePqMSIYZbKFuGtAmvd91F_7XiB7EuoN9SCHKhLkCCsx1L2X1ke2blh18xjL6t3jv11C5XEcAub-aF4mR74hLvWszpX-ExXnoUSZ_UBQiBNPy7DDNL04gHSnuqC2kOA5hR-na6ZUWrbrqtCgTtGNAhy5DpGJIOjsw0tU-hrD9rGbElmP7pbzVapAp9-SLXRbGbRnr2LtXtAH4rPc=">LinkedIn</a>.
Kura Oncology is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.&nbsp;
If you are a California resident, please see the attached Privacy Notice&nbsp;<a href="https://bit.ly/43vcIhg">CA Privacy Notice</a></div>

Director, Clinical Business Operatinos

<div class="content-intro">Are you ready to join a team committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines? At Kura Oncology, you have an opportunity to be a part of something bigger, with a lasting impact that you can be proud of.
At Kura Oncology, we are working to change the paradigm and improve the science of cancer treatment. As an organization, we strive to cultivate a diverse and talented professional culture driven to develop precision medicine therapeutics.
As we continue to build a leading biotech organization with a strong culture, a patient-focused mindset and a team focused on relentless execution, we are looking for innovative, passionate professionals to join us and make our vision a reality.
To succeed at Kura, you will need to have a demonstrated ability for excellence in drug discovery and development and a roll-up your sleeves attitude. The ideal candidate will possess a values-driven work style where integrity and grit drive all behaviors, decisions, and actions.</div>ESSENTIAL JOB FUNCTIONS:
Job Summary:
The Clinical Trial Associate (CTA) supports the operational execution of clinical trials from start-up through close-out. This role partners closely with Clinical Trial Leaders, study teams, CROs, and vendors to ensure trials are conducted efficiently, compliantly, and in alignment with program and company objectives.
Key Responsibilities
<ul>
<li>Support clinical trial operations across all phases of the study lifecycle, ensuring milestones, deliverables, timelines, and budgets are met.</li>
<li>Assist with CRO and vendor coordination and oversight, including tracking performance, deliverables, and documentation.</li>
<li>Collect, track, and review investigator site regulatory documentation (e.g., FDA Form 1572, FDFs, CVs, medical licenses, and study-specific documents) for completeness and accuracy.</li>
<li>Manage Trial Master File (TMF) filing, maintenance, reconciliation, and inspection readiness activities in compliance with ICH-GCP and company SOPs.</li>
<li>Track and maintain essential study documentation, including CTA and budget status, site and vendor payments, monitoring visits and reports, SUSARs, CAPAs, and enrollment metrics.</li>
<li>Coordinate study team, vendor, and site meetings, including scheduling, agenda preparation, minute-taking, and distribution.</li>
<li>Ensure clinical trial management systems (company and/or CRO systems) are kept current in collaboration with the Clinical Trial Leader (CTL).</li>
<li>Support study start-up, conduct, monitoring, and close-out activities to ensure protocol adherence and regulatory compliance.</li>
<li>Assist with site monitoring activities, audit and inspection preparation, and participate in audit/inspection interviews as required.</li>
<li>Support ordering, tracking, and distribution of investigational product and study supplies; assist with IRT oversight and drug inventory tracking.</li>
<li>Provide operational and financial support, including purchase orders, contract setup, invoice processing, and tracking of study budgets.</li>
<li>Assist with development, review, and maintenance of study documents (e.g., protocols, ICFs, CRFs, monitoring plans, manuals).</li>
<li>Review study reports and operational metrics for accuracy and quality.</li>
<li>Maintain study team lists, SUSAR distribution lists, databases, and departmental systems; support study team training activities.</li>
<li>Support inspection readiness, compliance activities, clinical trial insurance processes, and patient recruitment material review.</li>
<li>Collaborate cross-functionally with internal and external stakeholders to support successful trial execution.</li>
<li>Perform additional duties as assigned.</li>
<li>Experienced with using different eTMF systems (e.g., Veeva Vault, etc.)</li>
<li>Accountable for the quality of own work. Receives clear instruction, guidance and direction from more senior level roles or even solves problems of low complexity independently by identifying and selecting solutions and by analyzing factual information.</li>
<li>Contribute to harmonization of processes throughout Clinical Operations, use best practices to improve products or services</li>
<li>Contribute to process improvement suggestions</li>
<li>Take on additional tasks as assigned by management within a job discipline or specialized technical expertise</li>
</ul>
JOB SPECIFICATIONS:
<ul>
<li>Ability to work in a matrix environment</li>
<li>Experience working in a high-volume environment while maintaining both organization and the ability to prioritize tasks</li>
<li>Good understanding of the responsibilities and needs of other functions in a clinical trial</li>
<li>Reliable, conscientious, and confidential</li>
<li>Strong interpersonal skills and ability to deal with people at all levels with sensitivity and tact as well as ability to collaborate across</li>
<li>Some experience in oncology</li>
<li>Experience in CRO oversight is preferred.</li>
<li>Strong organization, documentation, and communication skills with an ability to</li>
<li>Ability to travel based on assigned study needs, typically minimal travel required.</li>
<li>Requires a bachelor’s degree in scientific field with no to some professional experienced or a substantial amount of professional experience in a clinical research-related position (1-2 years or equivalent) and/ or additional qualifications that also provides exposure to fundamental clinical research related skills &amp; knowledge</li>
<li>Good administrative and coordination skills</li>
<li>Good communication skills – both verbal and written</li>
<li>Good knowledge of medical and trial related terminology</li>
<li>Good oral and written communication in English, other languages an asset</li>
<li>Good organizational and problem-solving skills</li>
<li>Good time and priority management, ability to work efficiently under pressure</li>
<li>Good understanding of the policies and procedures of Clinical Operations and of ICH-GCP and current FDA regulations.</li>
<li>Motivated, shows initiative, is proactive and able to work independently as well as in a team</li>
<li>Strong computer skills including knowledge of MS Office™ (Excel™, Word™, PowerPoint™), Outlook, and TEAMS</li>
<li>Familiar with Trial Master File handling, including use of different eTMF systems</li>
<li>Willing to take on responsibility</li>
</ul>
The base range for this role is $85,000 - $98,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location, and relevant education or training. Kura's compensation package also includes generous benefits, equity, and participation in an annual target bonus.
#LI-RM1<div class="content-conclusion">Kura’s Values that are used for candidate selection and performance assessments:
<ul>
<li>We work as one for patients</li>
<li>We are goal-focused and deliver with excellence</li>
<li>We are science-driven courageous innovators</li>
<li>We strive to bring out the best in each other and ourselves</li>
</ul>
The Kura Package 
<ul>
<li>Career advancement/ development opportunities</li>
<li>Competitive comp package</li>
<li>Bonus</li>
<li>401K + Employer contributions</li>
<li>Generous stock options</li>
<li>ESPP Plan</li>
<li>20 days of PTO to start</li>
<li>18 Holidays&nbsp; (Including Summer &amp; Winter Break)</li>
<li>Generous Benefits Package with a variety of plans available with a substantial employer match</li>
<li>Paid Paternity/Maternity Leave</li>
<li>In-Office Catered lunches</li>
<li>Home Office Setup</li>
<li>Lifestyle Spending Stipend</li>
<li>Commuter Stipend (Boston Office)</li>
<li>Regular employee social activities, including happy hours, monthly birthday celebrations, Kura Koffee Talks, and much more!</li>
</ul>
Kura Oncology is a commercial-stage biopharmaceutical company committed to discovering and developing innovative precision medicines to help patients with cancer lead better, longer lives.
Through our deep understanding of cancer biology and decades of experience in precision oncology, we are studying the underlying causes of treatment resistance. This enables us to design smart combination regimens with other cancer therapies to target tumors from multiple directions, with the goal of improving long-term clinical benefit.
Kura developed and is commercializing KOMZIFTI® (ziftomenib), the FDA-approved once-daily, oral menin inhibitor for the treatment of adults with relapsed or refractory NPM1-mutated acute myeloid leukemia, and continues to pioneer advancements in menin inhibition and farnesyl transferase inhibition. For additional information, please visit Kura’s website at&nbsp;<a href="https://www.globenewswire.com/Tracker?data=ivPIaZ1M97sI-f2KN-08EdPH6mjSpiSN5KlK5_wlQbAAc4LWQocEKA9WUvb12WpwAN9k7iI4dL7FhQDxff_oY9qsBJJggCsRDLKBn9d-juCsq_E1nYXWUbPkipiFX7v6c5txgiRkYTmedLH_CMbGZGrwjGeppu4zTKTte98OnPG6O31YTGLfYCMEgU_q7Nda9e_0jwSblQw2MaRpdEflJOyNutWjOqPotKN5lxqDg-Y1UUF9H972qTWMlpwJdASFnH4jOkFTx4G1ePOUVApIr4lh_Q4tBul_A5aN9Go-704pV8GyzBO3XsQh6R2zmyotgeo7OJSsVJWiPMbdy8Xdpk0xIB81zv7DL1skxttlNuoVFX2_gQqD22FlIZX0eJTHeJ4_Im5HsRBZxO8iY08JPj9YO5W8wQjQbQGCEeCWAtJOzt79X-w9kpWvV30q2_Nv3_GHClF6m_ipTs6A3Dni9l8ihAggbB8JCtlahmKisZOERjyUz15eR5cyoeIbeX34hCzjvnsVJq2WYbfXyUWRcQ==">www.kuraoncology.com</a>&nbsp;and follow us on&nbsp;<a href="https://www.globenewswire.com/Tracker?data=0XrzPmD93VFEFgLaVr3RDXJ4YJ9GwVIrdBdEpaZqOXlWVFt2wNf-GaUGGD7vAJGfpHH18a0knFqQZ3VKcNbSrfyAweMLIwpkC8zrSNvFkBKLuOr_mnRS1Dq1TXP3--WW3ozJKzm5Tf2uvnAeJde-MlQBsDQieWSjNaw9g8uMPbWUxqjjWPc-YvQO5FjwEFspnPDZ7SsZ9Tj6xZxHPbhm0cG1woV_LAfBhUuAUorGYEwe1p023CEmpdHBqytB1Hb2Lca3QvrupWDzdPliVnBnazwblrZopi5a9BjP35irdevpYuevM0xDkPqhUbDaUOzsO8quAx--cMtliGWkIqyNO8BBXruqdidcb-dKXVzK9nnWNdBqNyJdnGJ_FKMNtSgvxpSjFm89EWwQk-2tCFVy-c3DiP3QOTNUsNZfdDvdalWiXA790TBE8-m6he3SH5kJE0jHosqjsWdQZ_LmmhF-APnsj5zLK30H9lJT_96t4y7taBZS9EgCbnKlIuMtg4Xt5QZ3XfY4a4QFzsKkZGcGZaOxBs148YXiBRrEMpHuVxm9Ed81NLoog4lyhe73Qdj3GJgvxI_UpHE9P2EWjVIO8wztEdDxd5kzg8Rbdp-HQ6fVkffcVZUaw1aYoJbRztrn9uzPu0qhXXcEooOlLAVcfA==">X</a>&nbsp;and&nbsp;<a href="https://www.globenewswire.com/Tracker?data=09ovKsXTlPV0n7MjNVrrRqAWBywJUeOxMzA_nYB0Mk0aAGczYB85764GV7bV1rte53dGawh5WyBhpHnXGI3ssuWm-1o-T3NalGIRz42ZpjYzyMPck9PFykD3kxqzRwUW5X1cNHoiCrfr5XfhWSBbdOWzC0i3dmxbxaPyBaKvqdJJIoR5mFg0YjYqYom9B-2uixJr1C2ZRKFqzkhKjPfkfPRiHu0QgJbQ8VPufnQc5Ac_860SJQLIG4kctJSyc1w4Ffp5NzgO0puLINW3Xsssd8lishssXKnQRc6IqzmMb3u1-FAJBoOauwh-pIEfxweaJy1Es3TEUOcN1aC0PFe8Cjp3IAkNSMq-1imazyxbc7QP4xj93QysOCLUdwT62O3Y4nP3TSl5cHBn2DIiUxW70gqQ04L2wUWgy14Tpl5CEYJ_Hp_JG3JIwh0SCWhbF7uPWoXfbcrK-jMjSsVM8JoNm7pt5tWA5e5m5iIFpNFP-Gn0zx9jrc3TinLD9ksPonmmf6uEP1loaxtKd5rIPeTu69E9mgnOePqMSIYZbKFuGtAmvd91F_7XiB7EuoN9SCHKhLkCCsx1L2X1ke2blh18xjL6t3jv11C5XEcAub-aF4mR74hLvWszpX-ExXnoUSZ_UBQiBNPy7DDNL04gHSnuqC2kOA5hR-na6ZUWrbrqtCgTtGNAhy5DpGJIOjsw0tU-hrD9rGbElmP7pbzVapAp9-SLXRbGbRnr2LtXtAH4rPc=">LinkedIn</a>.
Kura Oncology is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.&nbsp;
If you are a California resident, please see the attached Privacy Notice&nbsp;<a href="https://bit.ly/43vcIhg">CA Privacy Notice</a></div>

Clinical Trial Associate

<div class="content-intro">Are you ready to join a team committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines? At Kura Oncology, you have an opportunity to be a part of something bigger, with a lasting impact that you can be proud of.
At Kura Oncology, we are working to change the paradigm and improve the science of cancer treatment. As an organization, we strive to cultivate a diverse and talented professional culture driven to develop precision medicine therapeutics.
As we continue to build a leading biotech organization with a strong culture, a patient-focused mindset and a team focused on relentless execution, we are looking for innovative, passionate professionals to join us and make our vision a reality.
To succeed at Kura, you will need to have a demonstrated ability for excellence in drug discovery and development and a roll-up your sleeves attitude. The ideal candidate will possess a values-driven work style where integrity and grit drive all behaviors, decisions, and actions.</div><h2>ESSENTIAL JOB FUNCTIONS:</h2>
The Director, Medical Writing, serves as subject matter expert on clinical protocols, protocol amendments, clinical study reports, Investigator Brochures, and briefing books. The Director, Medical Writing may also provide guidance on document strategy for more complex dossiers for regulatory submission such as IND and NDA/BLA filings. The position requires the ability to work collaboratively with cross-functional teams in a fast-paced environment. The qualified candidate will also have experience in management of external vendors and the development of operational process improvements such as work practice documents, SOP development and updates, and document templates. There will need to be a very strong understanding of document timelines as planning is critical.
<ul>
<li>Serves as subject matter expert in preparing clinical regulatory documents through all phases clinical research.</li>
<li>Represent medical writing in cross-functional team meetings.</li>
<li>Collaborate with department heads and staff members of cross-functional groups, including clinical research, clinical operations, data management, biostatistics, regulatory affairs, and medical affairs as necessary to deliver documents with high quality on time.</li>
<li>Adhere to established regulatory standards, including ICH-E3 guidelines and company SOPs.</li>
<li>Support the development, improvement and maintenance of medical writing work practice documents, SOPs, and document templates to ensure consistency and efficiency.</li>
<li>Oversight of vendors including contract writers, QC reviewers, and document formatters.</li>
<li>Must have proficiency in the use of EndNote or RightFind Cite It software for the citation of literature references and creation of list of references in Word documents.</li>
<li>Maintain current knowledge of industry trends and best practices for medical writing.</li>
<li>Performs other duties as assigned</li>
</ul>
<h2>JOB SPECIFICATIONS:</h2>
<ul>
<li>Bachelor’s, Masters or PhD Degree in scientific, medical, clinical discipline or related field is required. Masters or Phd degree is preferred</li>
<li>A minimum of 10-12 years of relevant industry experience as a medical writer in a pharmaceutical, biotech, or CRO environment. Oncology experience preferred.</li>
<li>Must have experience authoring clinical study reports, protocols, protocol amendments, Investigator’s Brochure. Experience authoring and managing briefing books is a plus.</li>
<li>Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus</li>
<li>Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus</li>
<li>Project management skills as related to medical writing.</li>
<li>Ability to manage complex writing projects with minimal supervision.</li>
<li>Must have the ability to edit text for brevity and clarity.</li>
<li>Owns decision-making for their functional area or program, including resolving complex issues and making trade-offs to achieve program objectives, with minimal escalation.</li>
<li>Leads cross-functional collaboration for assigned programs, proactively driving alignment across stakeholders and resolving issues to support program execution.</li>
<li>Ability to understand, interpret and present complex clinical data.</li>
<li>Must be highly detail oriented.</li>
<li>Ability to coordinate multiple documents while effectively managing timelines.</li>
<li>High degree of independence in decision making and problem solving.</li>
<li>Understanding of FDA and ICH regulations and guidelines</li>
<li>Familiarity with eCTD-compliant templates and with the use of document formatting tools such as ISI writer, Liquent Smart Desk, Acumen Stylus, or other formatting tools.</li>
<li>Must be an expert with MS Word and have a solid working knowledge of MS Excel, MS PowerPoint, and MS Project.</li>
<li>Experience in use of an EDMS such as Documentum, Core Dossier, or Veeva.</li>
</ul>
The base range for an Associate Director is $182,000 - $211,000 and the Director level is $227,000 - $256,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location, and relevant education or training. Kura's compensation package also includes generous benefits, equity, and participation in an annual target bonus.<div class="content-conclusion">Kura’s Values that are used for candidate selection and performance assessments:
<ul>
<li>We work as one for patients</li>
<li>We are goal-focused and deliver with excellence</li>
<li>We are science-driven courageous innovators</li>
<li>We strive to bring out the best in each other and ourselves</li>
</ul>
The Kura Package 
<ul>
<li>Career advancement/ development opportunities</li>
<li>Competitive comp package</li>
<li>Bonus</li>
<li>401K + Employer contributions</li>
<li>Generous stock options</li>
<li>ESPP Plan</li>
<li>20 days of PTO to start</li>
<li>18 Holidays&nbsp; (Including Summer &amp; Winter Break)</li>
<li>Generous Benefits Package with a variety of plans available with a substantial employer match</li>
<li>Paid Paternity/Maternity Leave</li>
<li>In-Office Catered lunches</li>
<li>Home Office Setup</li>
<li>Lifestyle Spending Stipend</li>
<li>Commuter Stipend (Boston Office)</li>
<li>Regular employee social activities, including happy hours, monthly birthday celebrations, Kura Koffee Talks, and much more!</li>
</ul>
Kura Oncology is a commercial-stage biopharmaceutical company committed to discovering and developing innovative precision medicines to help patients with cancer lead better, longer lives.
Through our deep understanding of cancer biology and decades of experience in precision oncology, we are studying the underlying causes of treatment resistance. This enables us to design smart combination regimens with other cancer therapies to target tumors from multiple directions, with the goal of improving long-term clinical benefit.
Kura developed and is commercializing KOMZIFTI® (ziftomenib), the FDA-approved once-daily, oral menin inhibitor for the treatment of adults with relapsed or refractory NPM1-mutated acute myeloid leukemia, and continues to pioneer advancements in menin inhibition and farnesyl transferase inhibition. For additional information, please visit Kura’s website at&nbsp;<a href="https://www.globenewswire.com/Tracker?data=ivPIaZ1M97sI-f2KN-08EdPH6mjSpiSN5KlK5_wlQbAAc4LWQocEKA9WUvb12WpwAN9k7iI4dL7FhQDxff_oY9qsBJJggCsRDLKBn9d-juCsq_E1nYXWUbPkipiFX7v6c5txgiRkYTmedLH_CMbGZGrwjGeppu4zTKTte98OnPG6O31YTGLfYCMEgU_q7Nda9e_0jwSblQw2MaRpdEflJOyNutWjOqPotKN5lxqDg-Y1UUF9H972qTWMlpwJdASFnH4jOkFTx4G1ePOUVApIr4lh_Q4tBul_A5aN9Go-704pV8GyzBO3XsQh6R2zmyotgeo7OJSsVJWiPMbdy8Xdpk0xIB81zv7DL1skxttlNuoVFX2_gQqD22FlIZX0eJTHeJ4_Im5HsRBZxO8iY08JPj9YO5W8wQjQbQGCEeCWAtJOzt79X-w9kpWvV30q2_Nv3_GHClF6m_ipTs6A3Dni9l8ihAggbB8JCtlahmKisZOERjyUz15eR5cyoeIbeX34hCzjvnsVJq2WYbfXyUWRcQ==">www.kuraoncology.com</a>&nbsp;and follow us on&nbsp;<a href="https://www.globenewswire.com/Tracker?data=0XrzPmD93VFEFgLaVr3RDXJ4YJ9GwVIrdBdEpaZqOXlWVFt2wNf-GaUGGD7vAJGfpHH18a0knFqQZ3VKcNbSrfyAweMLIwpkC8zrSNvFkBKLuOr_mnRS1Dq1TXP3--WW3ozJKzm5Tf2uvnAeJde-MlQBsDQieWSjNaw9g8uMPbWUxqjjWPc-YvQO5FjwEFspnPDZ7SsZ9Tj6xZxHPbhm0cG1woV_LAfBhUuAUorGYEwe1p023CEmpdHBqytB1Hb2Lca3QvrupWDzdPliVnBnazwblrZopi5a9BjP35irdevpYuevM0xDkPqhUbDaUOzsO8quAx--cMtliGWkIqyNO8BBXruqdidcb-dKXVzK9nnWNdBqNyJdnGJ_FKMNtSgvxpSjFm89EWwQk-2tCFVy-c3DiP3QOTNUsNZfdDvdalWiXA790TBE8-m6he3SH5kJE0jHosqjsWdQZ_LmmhF-APnsj5zLK30H9lJT_96t4y7taBZS9EgCbnKlIuMtg4Xt5QZ3XfY4a4QFzsKkZGcGZaOxBs148YXiBRrEMpHuVxm9Ed81NLoog4lyhe73Qdj3GJgvxI_UpHE9P2EWjVIO8wztEdDxd5kzg8Rbdp-HQ6fVkffcVZUaw1aYoJbRztrn9uzPu0qhXXcEooOlLAVcfA==">X</a>&nbsp;and&nbsp;<a href="https://www.globenewswire.com/Tracker?data=09ovKsXTlPV0n7MjNVrrRqAWBywJUeOxMzA_nYB0Mk0aAGczYB85764GV7bV1rte53dGawh5WyBhpHnXGI3ssuWm-1o-T3NalGIRz42ZpjYzyMPck9PFykD3kxqzRwUW5X1cNHoiCrfr5XfhWSBbdOWzC0i3dmxbxaPyBaKvqdJJIoR5mFg0YjYqYom9B-2uixJr1C2ZRKFqzkhKjPfkfPRiHu0QgJbQ8VPufnQc5Ac_860SJQLIG4kctJSyc1w4Ffp5NzgO0puLINW3Xsssd8lishssXKnQRc6IqzmMb3u1-FAJBoOauwh-pIEfxweaJy1Es3TEUOcN1aC0PFe8Cjp3IAkNSMq-1imazyxbc7QP4xj93QysOCLUdwT62O3Y4nP3TSl5cHBn2DIiUxW70gqQ04L2wUWgy14Tpl5CEYJ_Hp_JG3JIwh0SCWhbF7uPWoXfbcrK-jMjSsVM8JoNm7pt5tWA5e5m5iIFpNFP-Gn0zx9jrc3TinLD9ksPonmmf6uEP1loaxtKd5rIPeTu69E9mgnOePqMSIYZbKFuGtAmvd91F_7XiB7EuoN9SCHKhLkCCsx1L2X1ke2blh18xjL6t3jv11C5XEcAub-aF4mR74hLvWszpX-ExXnoUSZ_UBQiBNPy7DDNL04gHSnuqC2kOA5hR-na6ZUWrbrqtCgTtGNAhy5DpGJIOjsw0tU-hrD9rGbElmP7pbzVapAp9-SLXRbGbRnr2LtXtAH4rPc=">LinkedIn</a>.
Kura Oncology is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.&nbsp;
If you are a California resident, please see the attached Privacy Notice&nbsp;<a href="https://bit.ly/43vcIhg">CA Privacy Notice</a></div>

Associate Director/Director, Medical & Regulatory Writing

<div class="content-intro">Are you ready to join a team committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines? At Kura Oncology, you have an opportunity to be a part of something bigger, with a lasting impact that you can be proud of.
At Kura Oncology, we are working to change the paradigm and improve the science of cancer treatment. As an organization, we strive to cultivate a diverse and talented professional culture driven to develop precision medicine therapeutics.
As we continue to build a leading biotech organization with a strong culture, a patient-focused mindset and a team focused on relentless execution, we are looking for innovative, passionate professionals to join us and make our vision a reality.
To succeed at Kura, you will need to have a demonstrated ability for excellence in drug discovery and development and a roll-up your sleeves attitude. The ideal candidate will possess a values-driven work style where integrity and grit drive all behaviors, decisions, and actions.</div>ESSENTIAL JOB FUNCTIONS:
The Applications Administrator / IT Business Partner (ITBP) is responsible for managing, optimizing, and supporting enterprise technology applications while partnering with business functions to align technology capabilities with organizational strategy and operational priorities. This role reports to the Executive Director of IT and serves as both a technical application administrator and a strategic liaison between the IT organization and business stakeholders/operations.
In this capacity, the role ensures enterprise applications are effectively implemented, configured, maintained, and supported while also identifying opportunities for technology-driven improvements across the organization. The ITBP works collaboratively with stakeholders to translate business needs into technology solutions, ensuring systems, platforms, and digital initiatives deliver measurable value to the organization.
Application Management
<ul>
<li>Oversee implementation, configuration, deployment, and lifecycle management of enterprise applications, platforms, and other business systems related to the Commercial organization.</li>
<li>Collaborate with stakeholders to configure and customize applications to meet evolving business requirements.</li>
<li>Manage and maintain SharePoint sites and implement platform changes to support the entire organization.</li>
<li>Coordinate system upgrades, patches, and maintenance to ensure optimal performance and security.</li>
<li>Partner with IT teams and external vendors to support integrations between enterprise systems and third-party solutions.</li>
</ul>
IT Business Partnership &amp; Strategic Alignment
<ul>
<li>Serve as an Information Technology Business Partner (ITBP) across the organization, aligning technology capabilities with business strategy and operational priorities.</li>
<li>Support strategic planning and technology roadmap development to ensure IT capabilities advance organizational growth and transformation. Act as a trusted advisor and liaison between functional leaders and the head of IT, fostering discovery and collaboration to align technology initiatives with enterprise objectives and Kura’s 2030 Vision.</li>
<li>Develop a deep understanding of organizational objectives, operational challenges, and emerging needs to translate them into scalable technology solutions.</li>
<li>Identify opportunities for digital enablement, automation, and process optimization.</li>
<li>Promote cross-functional collaboration between IT teams, functional stakeholders, and external partners to deliver effective technology solutions.</li>
<li>Advocate for business priorities within IT governance frameworks while ensuring alignment with security, compliance, and enterprise architecture standards.</li>
</ul>
Project &amp; Stakeholder Management
<ul>
<li>Facilitate project scoping, requirements gathering, and solution design in collaboration with stakeholders.</li>
<li>Develop user requirements, SOPs, and operational processes for supported systems.</li>
<li>Plan and execute assigned projects while monitoring progress and communicating status updates to leadership.</li>
<li>Coordinate testing, validation, and implementation activities to support system changes and enhancements.</li>
</ul>
User Support &amp; Training
<ul>
<li>Provide functional and technical support for enterprise applications.</li>
<li>Troubleshoot system issues and resolve user inquiries.</li>
<li>Develop and deliver training sessions, user documentation, and best practice guidance to improve system adoption.</li>
</ul>
Data &amp; System Governance
<ul>
<li>Manage system security including user access, roles, and permissions.</li>
<li>Ensure data integrity, accuracy, and consistency across enterprise systems.</li>
<li>Maintain compliance with company policies, SOX, GxP, and regulatory requirements.</li>
<li>Support system documentation, validation, and audit readiness activities.</li>
</ul>
Vendor &amp; Service Management
<ul>
<li>Serve as a primary contact for application vendors and service providers.</li>
<li>Coordinate vendor support, issue escalation, and service level management.</li>
<li>Collaborate with vendors and consulting partners to deliver system enhancements and upgrades.</li>
</ul>
Continuous Improvement &amp; Innovation
<ul>
<li>Identify opportunities to improve system functionality, user experience, and operational efficiency.</li>
<li>Evaluate emerging technologies and digital solutions that support organizational objectives.</li>
<li>Participate in innovation initiatives and pilot programs to enhance enterprise technology capabilities.</li>
</ul>
JOB SPECIFICATIONS:
<ul>
<li>Bachelor’s degree in a related technical or business discipline required.</li>
<li>A minimum of 6-8 years of progressive experience in IT leadership roles, with at least 5 years in management positions</li>
<li>Strategic IT and business alignment</li>
<li>Stakeholder relationship management</li>
<li>Enterprise application administration</li>
<li>Business process analysis and optimization</li>
<li>Project coordination and delivery</li>
<li>Vendor and service management</li>
<li>Technology governance and compliance</li>
<li>Communication and change management</li>
<li>Digital enablement and continuous improvement</li>
</ul>
The base range for this role is $165,000 - $195,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location, and relevant education or training. Kura's compensation package also includes generous benefits, equity, and participation in an annual target bonus.
#LI-RM1
&nbsp;<div class="content-conclusion">Kura’s Values that are used for candidate selection and performance assessments:
<ul>
<li>We work as one for patients</li>
<li>We are goal-focused and deliver with excellence</li>
<li>We are science-driven courageous innovators</li>
<li>We strive to bring out the best in each other and ourselves</li>
</ul>
The Kura Package 
<ul>
<li>Career advancement/ development opportunities</li>
<li>Competitive comp package</li>
<li>Bonus</li>
<li>401K + Employer contributions</li>
<li>Generous stock options</li>
<li>ESPP Plan</li>
<li>20 days of PTO to start</li>
<li>18 Holidays&nbsp; (Including Summer &amp; Winter Break)</li>
<li>Generous Benefits Package with a variety of plans available with a substantial employer match</li>
<li>Paid Paternity/Maternity Leave</li>
<li>In-Office Catered lunches</li>
<li>Home Office Setup</li>
<li>Lifestyle Spending Stipend</li>
<li>Commuter Stipend (Boston Office)</li>
<li>Regular employee social activities, including happy hours, monthly birthday celebrations, Kura Koffee Talks, and much more!</li>
</ul>
Kura Oncology is a commercial-stage biopharmaceutical company committed to discovering and developing innovative precision medicines to help patients with cancer lead better, longer lives.
Through our deep understanding of cancer biology and decades of experience in precision oncology, we are studying the underlying causes of treatment resistance. This enables us to design smart combination regimens with other cancer therapies to target tumors from multiple directions, with the goal of improving long-term clinical benefit.
Kura developed and is commercializing KOMZIFTI® (ziftomenib), the FDA-approved once-daily, oral menin inhibitor for the treatment of adults with relapsed or refractory NPM1-mutated acute myeloid leukemia, and continues to pioneer advancements in menin inhibition and farnesyl transferase inhibition. For additional information, please visit Kura’s website at&nbsp;<a href="https://www.globenewswire.com/Tracker?data=ivPIaZ1M97sI-f2KN-08EdPH6mjSpiSN5KlK5_wlQbAAc4LWQocEKA9WUvb12WpwAN9k7iI4dL7FhQDxff_oY9qsBJJggCsRDLKBn9d-juCsq_E1nYXWUbPkipiFX7v6c5txgiRkYTmedLH_CMbGZGrwjGeppu4zTKTte98OnPG6O31YTGLfYCMEgU_q7Nda9e_0jwSblQw2MaRpdEflJOyNutWjOqPotKN5lxqDg-Y1UUF9H972qTWMlpwJdASFnH4jOkFTx4G1ePOUVApIr4lh_Q4tBul_A5aN9Go-704pV8GyzBO3XsQh6R2zmyotgeo7OJSsVJWiPMbdy8Xdpk0xIB81zv7DL1skxttlNuoVFX2_gQqD22FlIZX0eJTHeJ4_Im5HsRBZxO8iY08JPj9YO5W8wQjQbQGCEeCWAtJOzt79X-w9kpWvV30q2_Nv3_GHClF6m_ipTs6A3Dni9l8ihAggbB8JCtlahmKisZOERjyUz15eR5cyoeIbeX34hCzjvnsVJq2WYbfXyUWRcQ==">www.kuraoncology.com</a>&nbsp;and follow us on&nbsp;<a href="https://www.globenewswire.com/Tracker?data=0XrzPmD93VFEFgLaVr3RDXJ4YJ9GwVIrdBdEpaZqOXlWVFt2wNf-GaUGGD7vAJGfpHH18a0knFqQZ3VKcNbSrfyAweMLIwpkC8zrSNvFkBKLuOr_mnRS1Dq1TXP3--WW3ozJKzm5Tf2uvnAeJde-MlQBsDQieWSjNaw9g8uMPbWUxqjjWPc-YvQO5FjwEFspnPDZ7SsZ9Tj6xZxHPbhm0cG1woV_LAfBhUuAUorGYEwe1p023CEmpdHBqytB1Hb2Lca3QvrupWDzdPliVnBnazwblrZopi5a9BjP35irdevpYuevM0xDkPqhUbDaUOzsO8quAx--cMtliGWkIqyNO8BBXruqdidcb-dKXVzK9nnWNdBqNyJdnGJ_FKMNtSgvxpSjFm89EWwQk-2tCFVy-c3DiP3QOTNUsNZfdDvdalWiXA790TBE8-m6he3SH5kJE0jHosqjsWdQZ_LmmhF-APnsj5zLK30H9lJT_96t4y7taBZS9EgCbnKlIuMtg4Xt5QZ3XfY4a4QFzsKkZGcGZaOxBs148YXiBRrEMpHuVxm9Ed81NLoog4lyhe73Qdj3GJgvxI_UpHE9P2EWjVIO8wztEdDxd5kzg8Rbdp-HQ6fVkffcVZUaw1aYoJbRztrn9uzPu0qhXXcEooOlLAVcfA==">X</a>&nbsp;and&nbsp;<a href="https://www.globenewswire.com/Tracker?data=09ovKsXTlPV0n7MjNVrrRqAWBywJUeOxMzA_nYB0Mk0aAGczYB85764GV7bV1rte53dGawh5WyBhpHnXGI3ssuWm-1o-T3NalGIRz42ZpjYzyMPck9PFykD3kxqzRwUW5X1cNHoiCrfr5XfhWSBbdOWzC0i3dmxbxaPyBaKvqdJJIoR5mFg0YjYqYom9B-2uixJr1C2ZRKFqzkhKjPfkfPRiHu0QgJbQ8VPufnQc5Ac_860SJQLIG4kctJSyc1w4Ffp5NzgO0puLINW3Xsssd8lishssXKnQRc6IqzmMb3u1-FAJBoOauwh-pIEfxweaJy1Es3TEUOcN1aC0PFe8Cjp3IAkNSMq-1imazyxbc7QP4xj93QysOCLUdwT62O3Y4nP3TSl5cHBn2DIiUxW70gqQ04L2wUWgy14Tpl5CEYJ_Hp_JG3JIwh0SCWhbF7uPWoXfbcrK-jMjSsVM8JoNm7pt5tWA5e5m5iIFpNFP-Gn0zx9jrc3TinLD9ksPonmmf6uEP1loaxtKd5rIPeTu69E9mgnOePqMSIYZbKFuGtAmvd91F_7XiB7EuoN9SCHKhLkCCsx1L2X1ke2blh18xjL6t3jv11C5XEcAub-aF4mR74hLvWszpX-ExXnoUSZ_UBQiBNPy7DDNL04gHSnuqC2kOA5hR-na6ZUWrbrqtCgTtGNAhy5DpGJIOjsw0tU-hrD9rGbElmP7pbzVapAp9-SLXRbGbRnr2LtXtAH4rPc=">LinkedIn</a>.
Kura Oncology is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.&nbsp;
If you are a California resident, please see the attached Privacy Notice&nbsp;<a href="https://bit.ly/43vcIhg">CA Privacy Notice</a></div>

Applications Administrator / IT Business Partner

<div class="content-intro">Are you ready to join a team committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines? At Kura Oncology, you have an opportunity to be a part of something bigger, with a lasting impact that you can be proud of.
At Kura Oncology, we are working to change the paradigm and improve the science of cancer treatment. As an organization, we strive to cultivate a diverse and talented professional culture driven to develop precision medicine therapeutics.
As we continue to build a leading biotech organization with a strong culture, a patient-focused mindset and a team focused on relentless execution, we are looking for innovative, passionate professionals to join us and make our vision a reality.
To succeed at Kura, you will need to have a demonstrated ability for excellence in drug discovery and development and a roll-up your sleeves attitude. The ideal candidate will possess a values-driven work style where integrity and grit drive all behaviors, decisions, and actions.</div>Reporting to the Regional Business Director, the Oncology Account Manager (OAM) will contribute to Kura’s overall sales objective by performing assigned sales related activities. The OAM will provide physicians, pharmacists, nurses and all healthcare professionals (HCPs) with product, services and approved information that will enable the HCPs to appropriately prescribe Kura’s product(s)The OAM will compliantly and successfully implement Kura’s marketing strategies and corresponding tactics in order to achieve short-term and long-term objectives. The ideal candidate will be capable of managing the territory and administrative requirements in an efficient and effective manner and will achieve full compliance with drug laws and regulations when representing Kura and Kura’s products to Healthcare Providers.&nbsp;
ESSENTIAL JOB FUNCTIONS:
<ul>
<li>Achieve the assigned sales objective for the territory</li>
<li>Attain the designated goals for calls on appropriate healthcare professionals to communicate balanced, accurate, and complete information on Kura’s FDA approved products</li>
<li>Develops and implements a territory business plan to meet customer needs and achieve goals</li>
<li>Navigate through complex external/customer organizational structures including hospitals, IDNs, GPOs and healthcare communities while aligning with cross-functional commercial partners</li>
<li>Demonstrate completion of administrative requirements including budget management, expense reports management, CRM call reporting and synchronization, etc. within timelines and company guidelines</li>
<li>Demonstrates a deep understanding of healthcare professionals (HCP) and account needs, effectively utilizing this knowledge to strategically promote and expand the use of assigned products</li>
<li>Operate the territory within the assigned expense budget and demonstrates fiscal responsibility</li>
<li>Comply with all federal/state/local laws, regulations and guidelines including but not limited to the PhRMA Code on Interactions with Healthcare Professionals as well as complying with all Kura standards and policies relating to all job activities</li>
<li>Successful completion and ongoing updates of all aspects of training including but not limited to product knowledge, disease state, market, selling skills and compliance</li>
<li>Assists in the identification and resolution of issues and opportunities while communicating proactively to marketing and sales management</li>
<li>Develops and consistently demonstrates an expert understanding of HCP and Account needs to appropriately expand use of assigned product.&nbsp;</li>
</ul>
JOB SPECIFICATIONS:
<ul>
<li>Undergraduate degree required, ideally in business/marketing/healthcare/life science areas of concentration</li>
<li>6+ years of successful pharmaceutical/biotech sales experience with 3+ in the oncology/hematology and/or rare disease markets, preferably with oral therapeutic selling experience</li>
<li>Management of large territories that includes periodic overnight travel</li>
<li>Occasionally work evenings and weekends as needed for conferences</li>
<li>Excellent written and oral communication skills</li>
<li>Strong computer skills, notably WORD, EXCEL and POWER POINT</li>
</ul>
The base range for this role is $205,000 to $230,000 per year with a target IC of 60k. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location, and relevant education or training. Kura's compensation package also includes generous benefits, equity, and participation in an annual target bonus.
&nbsp;<div class="content-conclusion">Kura’s Values that are used for candidate selection and performance assessments:
<ul>
<li>We work as one for patients</li>
<li>We are goal-focused and deliver with excellence</li>
<li>We are science-driven courageous innovators</li>
<li>We strive to bring out the best in each other and ourselves</li>
</ul>
The Kura Package 
<ul>
<li>Career advancement/ development opportunities</li>
<li>Competitive comp package</li>
<li>Bonus</li>
<li>401K + Employer contributions</li>
<li>Generous stock options</li>
<li>ESPP Plan</li>
<li>20 days of PTO to start</li>
<li>18 Holidays&nbsp; (Including Summer &amp; Winter Break)</li>
<li>Generous Benefits Package with a variety of plans available with a substantial employer match</li>
<li>Paid Paternity/Maternity Leave</li>
<li>In-Office Catered lunches</li>
<li>Home Office Setup</li>
<li>Lifestyle Spending Stipend</li>
<li>Commuter Stipend (Boston Office)</li>
<li>Regular employee social activities, including happy hours, monthly birthday celebrations, Kura Koffee Talks, and much more!</li>
</ul>
Kura Oncology is a commercial-stage biopharmaceutical company committed to discovering and developing innovative precision medicines to help patients with cancer lead better, longer lives.
Through our deep understanding of cancer biology and decades of experience in precision oncology, we are studying the underlying causes of treatment resistance. This enables us to design smart combination regimens with other cancer therapies to target tumors from multiple directions, with the goal of improving long-term clinical benefit.
Kura developed and is commercializing KOMZIFTI® (ziftomenib), the FDA-approved once-daily, oral menin inhibitor for the treatment of adults with relapsed or refractory NPM1-mutated acute myeloid leukemia, and continues to pioneer advancements in menin inhibition and farnesyl transferase inhibition. For additional information, please visit Kura’s website at&nbsp;<a href="https://www.globenewswire.com/Tracker?data=ivPIaZ1M97sI-f2KN-08EdPH6mjSpiSN5KlK5_wlQbAAc4LWQocEKA9WUvb12WpwAN9k7iI4dL7FhQDxff_oY9qsBJJggCsRDLKBn9d-juCsq_E1nYXWUbPkipiFX7v6c5txgiRkYTmedLH_CMbGZGrwjGeppu4zTKTte98OnPG6O31YTGLfYCMEgU_q7Nda9e_0jwSblQw2MaRpdEflJOyNutWjOqPotKN5lxqDg-Y1UUF9H972qTWMlpwJdASFnH4jOkFTx4G1ePOUVApIr4lh_Q4tBul_A5aN9Go-704pV8GyzBO3XsQh6R2zmyotgeo7OJSsVJWiPMbdy8Xdpk0xIB81zv7DL1skxttlNuoVFX2_gQqD22FlIZX0eJTHeJ4_Im5HsRBZxO8iY08JPj9YO5W8wQjQbQGCEeCWAtJOzt79X-w9kpWvV30q2_Nv3_GHClF6m_ipTs6A3Dni9l8ihAggbB8JCtlahmKisZOERjyUz15eR5cyoeIbeX34hCzjvnsVJq2WYbfXyUWRcQ==">www.kuraoncology.com</a>&nbsp;and follow us on&nbsp;<a href="https://www.globenewswire.com/Tracker?data=0XrzPmD93VFEFgLaVr3RDXJ4YJ9GwVIrdBdEpaZqOXlWVFt2wNf-GaUGGD7vAJGfpHH18a0knFqQZ3VKcNbSrfyAweMLIwpkC8zrSNvFkBKLuOr_mnRS1Dq1TXP3--WW3ozJKzm5Tf2uvnAeJde-MlQBsDQieWSjNaw9g8uMPbWUxqjjWPc-YvQO5FjwEFspnPDZ7SsZ9Tj6xZxHPbhm0cG1woV_LAfBhUuAUorGYEwe1p023CEmpdHBqytB1Hb2Lca3QvrupWDzdPliVnBnazwblrZopi5a9BjP35irdevpYuevM0xDkPqhUbDaUOzsO8quAx--cMtliGWkIqyNO8BBXruqdidcb-dKXVzK9nnWNdBqNyJdnGJ_FKMNtSgvxpSjFm89EWwQk-2tCFVy-c3DiP3QOTNUsNZfdDvdalWiXA790TBE8-m6he3SH5kJE0jHosqjsWdQZ_LmmhF-APnsj5zLK30H9lJT_96t4y7taBZS9EgCbnKlIuMtg4Xt5QZ3XfY4a4QFzsKkZGcGZaOxBs148YXiBRrEMpHuVxm9Ed81NLoog4lyhe73Qdj3GJgvxI_UpHE9P2EWjVIO8wztEdDxd5kzg8Rbdp-HQ6fVkffcVZUaw1aYoJbRztrn9uzPu0qhXXcEooOlLAVcfA==">X</a>&nbsp;and&nbsp;<a href="https://www.globenewswire.com/Tracker?data=09ovKsXTlPV0n7MjNVrrRqAWBywJUeOxMzA_nYB0Mk0aAGczYB85764GV7bV1rte53dGawh5WyBhpHnXGI3ssuWm-1o-T3NalGIRz42ZpjYzyMPck9PFykD3kxqzRwUW5X1cNHoiCrfr5XfhWSBbdOWzC0i3dmxbxaPyBaKvqdJJIoR5mFg0YjYqYom9B-2uixJr1C2ZRKFqzkhKjPfkfPRiHu0QgJbQ8VPufnQc5Ac_860SJQLIG4kctJSyc1w4Ffp5NzgO0puLINW3Xsssd8lishssXKnQRc6IqzmMb3u1-FAJBoOauwh-pIEfxweaJy1Es3TEUOcN1aC0PFe8Cjp3IAkNSMq-1imazyxbc7QP4xj93QysOCLUdwT62O3Y4nP3TSl5cHBn2DIiUxW70gqQ04L2wUWgy14Tpl5CEYJ_Hp_JG3JIwh0SCWhbF7uPWoXfbcrK-jMjSsVM8JoNm7pt5tWA5e5m5iIFpNFP-Gn0zx9jrc3TinLD9ksPonmmf6uEP1loaxtKd5rIPeTu69E9mgnOePqMSIYZbKFuGtAmvd91F_7XiB7EuoN9SCHKhLkCCsx1L2X1ke2blh18xjL6t3jv11C5XEcAub-aF4mR74hLvWszpX-ExXnoUSZ_UBQiBNPy7DDNL04gHSnuqC2kOA5hR-na6ZUWrbrqtCgTtGNAhy5DpGJIOjsw0tU-hrD9rGbElmP7pbzVapAp9-SLXRbGbRnr2LtXtAH4rPc=">LinkedIn</a>.
Kura Oncology is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.&nbsp;
If you are a California resident, please see the attached Privacy Notice&nbsp;<a href="https://bit.ly/43vcIhg">CA Privacy Notice</a></div>

Oncology Account Manager - Indianapolis/KY/IL

<div class="content-intro">Are you ready to join a team committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines? At Kura Oncology, you have an opportunity to be a part of something bigger, with a lasting impact that you can be proud of.
At Kura Oncology, we are working to change the paradigm and improve the science of cancer treatment. As an organization, we strive to cultivate a diverse and talented professional culture driven to develop precision medicine therapeutics.
As we continue to build a leading biotech organization with a strong culture, a patient-focused mindset and a team focused on relentless execution, we are looking for innovative, passionate professionals to join us and make our vision a reality.
To succeed at Kura, you will need to have a demonstrated ability for excellence in drug discovery and development and a roll-up your sleeves attitude. The ideal candidate will possess a values-driven work style where integrity and grit drive all behaviors, decisions, and actions.</div>ESSENTIAL JOB FUNCTIONS:
<ul>
<li>Leads the Quality Unit responsible for Good Clinical Practices (GCP), Good Laboratory Practices (GLP), Good Manufacturing Practices (cGMP), Good Pharmacovigilance Practices (GVP), and Computer Software Validation (CSV).</li>
<li>Develops, implements, and manages the Quality System to the standards expected by Health Authorities to support clinical development, commercial operations, and the post-approval product lifecycle.</li>
<li>Commercial product disposition and end-to-end quality oversight of manufacturing, testing, packaging, labeling, storage, and distribution activities.</li>
<li>Governance and quality oversight of the commercial supplier network, including CMOs, contract laboratories, packagers, distributors, 3PLs, and applicable specialty-pharmacy partners.</li>
<li>Oversight of the commercial product quality lifecycle, including product complaints, investigations, returns, field alert reports, recalls, market actions, and counterfeit or product-integrity concerns.</li>
<li>Provides Quality oversight for internal GCP, GMP, GLP, and GVP activities.</li>
<li>Ensures appropriate Quality oversight of CMOs, laboratories, suppliers, packagers, distributors, 3PLs, and alliance partners</li>
<li>Leads Inspection Readiness and/or Inspection Preparedness efforts.</li>
<li>Acts as lead/Host contact for GxP site inspections.</li>
<li>Manages Quality System Reviews and presents to Management.</li>
<li>Evaluates GxP activities for continuous improvement opportunities to the Quality System.</li>
<li>Ensures risk-based quality management (RBQM) is applied as appropriate to clinical studies.</li>
<li>Manages critical GxP product-quality, data-integrity, safety, and compliance events</li>
<li>Identifies potential Quality risks to strategic and/or operational plans and proposes options to mitigate risks.</li>
<li>Manages GxP Quality personnel, activities, and budget.</li>
</ul>
JOB SPECIFICATIONS:
<ul>
<li>Bachelor’s degree in a Life Sciences discipline or equivalent.</li>
<li>A minimum of 18 years of relevant experience in a regulated biotech, or pharmaceutical industry in a Quality Assurance function.</li>
<li>Clinical development, commercial launch, and marketed-product lifecycle experience with strong experience supporting NDA approvals, MAAs, commercial launches, and post-approval submissions</li>
<li>Experience with developing, implementing, and maintaining GxP Quality System which ensures compliance to GxP and regulatory standards.</li>
<li>Experience in managing, hosting and/or supporting Health Authority inspections.</li>
<li>Demonstrates proven track record of leadership, communication, and motivation skills with internal and external Vendors.</li>
<li>A strong team player with the ability to effectively communicate sound quality advice cross-functionally based on experience, regulations, and business needs.</li>
<li>Provide solutions to issues. Solutions are imaginative, thorough, practical, and consistent with objectives.</li>
<li>Solves conflict and addresses workplace issues in professional and collaborative manner.</li>
<li>Flexibility and ability to provide a solution-based approach to emerging challenges and changing priorities.</li>
<li>Clear, concise writing skills and good verbal presentation skills.</li>
<li>Self-motivated, detail oriented, well organized, and able to demonstrate success with managing multiple projects simultaneously and other priorities.</li>
<li>Ability to interact constructively and efficiently with co-workers within and across departments, Management, and Vendors.</li>
<li>Owns and makes final decisions for the function, including those with significant impact on portfolio strategy, organizational priorities, and business outcomes.</li>
<li>Leads cross-functional alignment at the executive level, partnering with senior leaders to drive integrated strategy and ensure execution against enterprise priorities.</li>
<li>Communicate decisions and recommendations with clear justification.</li>
<li>Ability to resolve day-to-day issues efficiently while maintaining compliance.</li>
<li>Independently determines and develops approach to solutions.</li>
<li>Proficient in Veeva QualityDocs.</li>
<li>Proficient in Word, Excel, PowerPoint, SharePoint.</li>
<li>Ability to travel for both domestic and international business.</li>
</ul>
The base range for a Vice President is $325,000 - $372,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location, and relevant education or training. Kura's compensation package also includes generous benefits, equity, and participation in an annual target bonus.
#LI-RM1<div class="content-conclusion">Kura’s Values that are used for candidate selection and performance assessments:
<ul>
<li>We work as one for patients</li>
<li>We are goal-focused and deliver with excellence</li>
<li>We are science-driven courageous innovators</li>
<li>We strive to bring out the best in each other and ourselves</li>
</ul>
The Kura Package 
<ul>
<li>Career advancement/ development opportunities</li>
<li>Competitive comp package</li>
<li>Bonus</li>
<li>401K + Employer contributions</li>
<li>Generous stock options</li>
<li>ESPP Plan</li>
<li>20 days of PTO to start</li>
<li>18 Holidays&nbsp; (Including Summer &amp; Winter Break)</li>
<li>Generous Benefits Package with a variety of plans available with a substantial employer match</li>
<li>Paid Paternity/Maternity Leave</li>
<li>In-Office Catered lunches</li>
<li>Home Office Setup</li>
<li>Lifestyle Spending Stipend</li>
<li>Commuter Stipend (Boston Office)</li>
<li>Regular employee social activities, including happy hours, monthly birthday celebrations, Kura Koffee Talks, and much more!</li>
</ul>
Kura Oncology is a commercial-stage biopharmaceutical company committed to discovering and developing innovative precision medicines to help patients with cancer lead better, longer lives.
Through our deep understanding of cancer biology and decades of experience in precision oncology, we are studying the underlying causes of treatment resistance. This enables us to design smart combination regimens with other cancer therapies to target tumors from multiple directions, with the goal of improving long-term clinical benefit.
Kura developed and is commercializing KOMZIFTI® (ziftomenib), the FDA-approved once-daily, oral menin inhibitor for the treatment of adults with relapsed or refractory NPM1-mutated acute myeloid leukemia, and continues to pioneer advancements in menin inhibition and farnesyl transferase inhibition. For additional information, please visit Kura’s website at&nbsp;<a href="https://www.globenewswire.com/Tracker?data=ivPIaZ1M97sI-f2KN-08EdPH6mjSpiSN5KlK5_wlQbAAc4LWQocEKA9WUvb12WpwAN9k7iI4dL7FhQDxff_oY9qsBJJggCsRDLKBn9d-juCsq_E1nYXWUbPkipiFX7v6c5txgiRkYTmedLH_CMbGZGrwjGeppu4zTKTte98OnPG6O31YTGLfYCMEgU_q7Nda9e_0jwSblQw2MaRpdEflJOyNutWjOqPotKN5lxqDg-Y1UUF9H972qTWMlpwJdASFnH4jOkFTx4G1ePOUVApIr4lh_Q4tBul_A5aN9Go-704pV8GyzBO3XsQh6R2zmyotgeo7OJSsVJWiPMbdy8Xdpk0xIB81zv7DL1skxttlNuoVFX2_gQqD22FlIZX0eJTHeJ4_Im5HsRBZxO8iY08JPj9YO5W8wQjQbQGCEeCWAtJOzt79X-w9kpWvV30q2_Nv3_GHClF6m_ipTs6A3Dni9l8ihAggbB8JCtlahmKisZOERjyUz15eR5cyoeIbeX34hCzjvnsVJq2WYbfXyUWRcQ==">www.kuraoncology.com</a>&nbsp;and follow us on&nbsp;<a href="https://www.globenewswire.com/Tracker?data=0XrzPmD93VFEFgLaVr3RDXJ4YJ9GwVIrdBdEpaZqOXlWVFt2wNf-GaUGGD7vAJGfpHH18a0knFqQZ3VKcNbSrfyAweMLIwpkC8zrSNvFkBKLuOr_mnRS1Dq1TXP3--WW3ozJKzm5Tf2uvnAeJde-MlQBsDQieWSjNaw9g8uMPbWUxqjjWPc-YvQO5FjwEFspnPDZ7SsZ9Tj6xZxHPbhm0cG1woV_LAfBhUuAUorGYEwe1p023CEmpdHBqytB1Hb2Lca3QvrupWDzdPliVnBnazwblrZopi5a9BjP35irdevpYuevM0xDkPqhUbDaUOzsO8quAx--cMtliGWkIqyNO8BBXruqdidcb-dKXVzK9nnWNdBqNyJdnGJ_FKMNtSgvxpSjFm89EWwQk-2tCFVy-c3DiP3QOTNUsNZfdDvdalWiXA790TBE8-m6he3SH5kJE0jHosqjsWdQZ_LmmhF-APnsj5zLK30H9lJT_96t4y7taBZS9EgCbnKlIuMtg4Xt5QZ3XfY4a4QFzsKkZGcGZaOxBs148YXiBRrEMpHuVxm9Ed81NLoog4lyhe73Qdj3GJgvxI_UpHE9P2EWjVIO8wztEdDxd5kzg8Rbdp-HQ6fVkffcVZUaw1aYoJbRztrn9uzPu0qhXXcEooOlLAVcfA==">X</a>&nbsp;and&nbsp;<a href="https://www.globenewswire.com/Tracker?data=09ovKsXTlPV0n7MjNVrrRqAWBywJUeOxMzA_nYB0Mk0aAGczYB85764GV7bV1rte53dGawh5WyBhpHnXGI3ssuWm-1o-T3NalGIRz42ZpjYzyMPck9PFykD3kxqzRwUW5X1cNHoiCrfr5XfhWSBbdOWzC0i3dmxbxaPyBaKvqdJJIoR5mFg0YjYqYom9B-2uixJr1C2ZRKFqzkhKjPfkfPRiHu0QgJbQ8VPufnQc5Ac_860SJQLIG4kctJSyc1w4Ffp5NzgO0puLINW3Xsssd8lishssXKnQRc6IqzmMb3u1-FAJBoOauwh-pIEfxweaJy1Es3TEUOcN1aC0PFe8Cjp3IAkNSMq-1imazyxbc7QP4xj93QysOCLUdwT62O3Y4nP3TSl5cHBn2DIiUxW70gqQ04L2wUWgy14Tpl5CEYJ_Hp_JG3JIwh0SCWhbF7uPWoXfbcrK-jMjSsVM8JoNm7pt5tWA5e5m5iIFpNFP-Gn0zx9jrc3TinLD9ksPonmmf6uEP1loaxtKd5rIPeTu69E9mgnOePqMSIYZbKFuGtAmvd91F_7XiB7EuoN9SCHKhLkCCsx1L2X1ke2blh18xjL6t3jv11C5XEcAub-aF4mR74hLvWszpX-ExXnoUSZ_UBQiBNPy7DDNL04gHSnuqC2kOA5hR-na6ZUWrbrqtCgTtGNAhy5DpGJIOjsw0tU-hrD9rGbElmP7pbzVapAp9-SLXRbGbRnr2LtXtAH4rPc=">LinkedIn</a>.
Kura Oncology is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.&nbsp;
If you are a California resident, please see the attached Privacy Notice&nbsp;<a href="https://bit.ly/43vcIhg">CA Privacy Notice</a></div>

Vice President, Quality Assurance

<div class="content-intro">Are you ready to join a team committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines? At Kura Oncology, you have an opportunity to be a part of something bigger, with a lasting impact that you can be proud of.
At Kura Oncology, we are working to change the paradigm and improve the science of cancer treatment. As an organization, we strive to cultivate a diverse and talented professional culture driven to develop precision medicine therapeutics.
As we continue to build a leading biotech organization with a strong culture, a patient-focused mindset and a team focused on relentless execution, we are looking for innovative, passionate professionals to join us and make our vision a reality.
To succeed at Kura, you will need to have a demonstrated ability for excellence in drug discovery and development and a roll-up your sleeves attitude. The ideal candidate will possess a values-driven work style where integrity and grit drive all behaviors, decisions, and actions.</div><h2>ESSENTIAL JOB FUNCTIONS:</h2>
The Associate Director, Medical &amp; Regulatory Writing serves as a subject matter expert in the writing and production of clinical documents such as the writing of clinical protocols, protocol amendments, clinical study reports, Investigator’s Brochures, and briefing books. This role is also accountable for Clinical Trial Transparency &amp; Disclosure (CTD) responsibilities and oversight of vendors carrying out such work. The position requires the ability to work collaboratively with cross-functional teams in a fast-paced environment. The qualified candidate will also have experience in oversight of external vendors. There needs to be a very strong understanding of document timelines as planning is critical.
<ul>
<li>Serves as the assigned medical writer and subject matter expert in preparing clinical regulatory documents through all phases of clinical research.</li>
<li>Execute clinical trials transparency and disclosures (CTD) book of work and provide vendor oversight</li>
<li>Collaborates with the cross-functional team comprised of regulatory affairs, clinical development, clinical operations, biostatistics, pharmacology, translational research, manufacturing, etc. to interpret study results and ensure study results and statistical interpretations are accurately and clearly reflected in relevant documents.</li>
<li>Manages the document review process ensuring conflicting and/or ambiguous comments are clarified and appropriately addressed.</li>
<li>Works closely with the study team to reach consensus on timelines for deliverables.</li>
<li>Completes documents according to agreed-upon timelines for deliverables and follows up with the study team as needed to meet timeline commitments.</li>
<li>Adhere to established regulatory standards, including ICH-E3 guidelines and company SOPs.</li>
<li>Support the development, improvement and maintenance of regulatory and scientific writing work practice documents, SOPs, and document templates to ensure consistency and efficiency.</li>
<li>Represent medical writing in cross-functional team meetings.</li>
<li>Collaborate with department heads and staff members of cross-functional groups, including clinical development, clinical operations, data management, biostatistics, regulatory affairs, and medical affairs as necessary to deliver documents with high quality on time.</li>
<li>Adhere to established regulatory standards, including ICH-E3 guidelines and company SOPs.</li>
<li>Support the development, improvement and maintenance of medical writing work practice documents, SOPs, and document templates to ensure consistency and efficiency.</li>
<li>Lead the development of overall global clinical trials transparency and disclosures policy with key stakeholders, updating the policy as necessary</li>
<li>Lead teams in the preparation and maintenance of CCI and PPD rules across programs, ensuring consistency of publicly disclosed information across countries, websites, databases, and documents</li>
<li>Ensure lean writing practices for regulatory documents such as Clinical Trial Protocols, Investigator's Brochures, Informed Consent templates and Clinical Study Reports to minimize CCI and PPD</li>
<li>Analyze, validate, and prioritize complex and dynamic information from a diverse range of sources in response to technical and operational challenges</li>
<li>Manage, track and present assigned book-of-work, compile and report performance metrics</li>
<li>Manage the preparation of plain language (layperson) synopses and summaries and redaction of clinical documents in accordance with FDA requirements, EMA Policy 0070, EU Clinical Trial Regulation, Health Canada Public Release of Clinical Information (PRCI), and other global regulations</li>
<li>Educate and provide company-wide awareness of transparency/disclosure regulations and industry trends, as well as requirements for layperson summaries and clinical study diversity planning.</li>
<li>Coordinate efforts of cross-functional teams to produce documents &amp; postings (e.g., plain language (layperson) summaries, interim and/or results postings, and redaction documents), acting as liaison between the vendor and internal teams</li>
<li>For relevant trials, collaborate with internal and external stakeholders to develop and implement diversity action plans in accordance with FDA guidance</li>
<li>Work on multiple projects/across programs, coordinating work plans that align with corporate timelines and strategic plans</li>
<li>Oversight of vendors in the Clinical trial transparency and disclosure space</li>
<li>Must have proficiency in the use of Veeva or equivalent It software for document creation, review, and QC including applications for citation of literature references and creation of list of references in Word documents.</li>
<li>Maintain current knowledge of industry trends and best practices for medical writing.</li>
<li>Performs other duties as assigned</li>
</ul>
<h2>JOB SPECIFICATIONS:</h2>
<ul>
<li>Masters or advanced degree in scientific, medical, or clinical discipline (eg, PhD, PharmD, or equivalent) is required. PhD degree is preferred.</li>
<li>Must have a minimum of 8-10 years of relevant industry experience as a regulatory/scientific writer in a pharmaceutical, biotech, or CRO environment. Must have CTD experience, vendor oversight a plus. Oncology experience preferred.</li>
<li>Must have experience authoring clinical study reports, protocols, protocol amendments, Investigator’s Brochures. Experience authoring briefing books and Module 2 clinical summaries (2.5, 2.7.3, 2.7.4) is a plus.</li>
<li>Ability to work effectively in a collaborative team environment where results are achieved through influence, cooperation, and the incorporation of multiple points of view.</li>
<li>Solid understanding of drug development, clinical research, data analysis, Common Technical Document (CTD), ICH guidelines, GxP, regulatory interactions, and relevant regulations, requirements and guidance associated with document preparation and submission.</li>
<li>Ability to manage competing priorities in a fast-paced environment.</li>
<li>Excellent problem solving, organizational, and analytical critical thinking skills.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Strong attention to detail related to consistency, grammar, syntax, and formatting.</li>
<li>Familiarity with eCTD-compliant templates and with the use of document formatting tools such as ISI writer, Liquent Smart Desk, Acumen Stylus, or other formatting tools is a plus.</li>
<li>Proficient in MS Office Suite, EndNote, and Adobe Acrobat.</li>
<li>Experience with use of an EDMS such as Documentum, Core Dossier, or Veeva.</li>
<li>Ability to travel up to approximately 10% of the time.</li>
<li>Makes decisions for assigned programs or functional areas, balancing priorities and resolving routine challenges; escalates high-impact or cross-functional decisions as needed.</li>
<li>Facilitates cross-functional coordination for assigned programs or initiatives, ensuring alignment and timely execution of deliverables.</li>
</ul>
The base range for an Associate Director is $184,000 - $211,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location, and relevant education or training. Kura's compensation package also includes generous benefits, equity, and participation in an annual target bonus.<div class="content-conclusion">Kura’s Values that are used for candidate selection and performance assessments:
<ul>
<li>We work as one for patients</li>
<li>We are goal-focused and deliver with excellence</li>
<li>We are science-driven courageous innovators</li>
<li>We strive to bring out the best in each other and ourselves</li>
</ul>
The Kura Package 
<ul>
<li>Career advancement/ development opportunities</li>
<li>Competitive comp package</li>
<li>Bonus</li>
<li>401K + Employer contributions</li>
<li>Generous stock options</li>
<li>ESPP Plan</li>
<li>20 days of PTO to start</li>
<li>18 Holidays&nbsp; (Including Summer &amp; Winter Break)</li>
<li>Generous Benefits Package with a variety of plans available with a substantial employer match</li>
<li>Paid Paternity/Maternity Leave</li>
<li>In-Office Catered lunches</li>
<li>Home Office Setup</li>
<li>Lifestyle Spending Stipend</li>
<li>Commuter Stipend (Boston Office)</li>
<li>Regular employee social activities, including happy hours, monthly birthday celebrations, Kura Koffee Talks, and much more!</li>
</ul>
Kura Oncology is a commercial-stage biopharmaceutical company committed to discovering and developing innovative precision medicines to help patients with cancer lead better, longer lives.
Through our deep understanding of cancer biology and decades of experience in precision oncology, we are studying the underlying causes of treatment resistance. This enables us to design smart combination regimens with other cancer therapies to target tumors from multiple directions, with the goal of improving long-term clinical benefit.
Kura developed and is commercializing KOMZIFTI® (ziftomenib), the FDA-approved once-daily, oral menin inhibitor for the treatment of adults with relapsed or refractory NPM1-mutated acute myeloid leukemia, and continues to pioneer advancements in menin inhibition and farnesyl transferase inhibition. For additional information, please visit Kura’s website at&nbsp;<a href="https://www.globenewswire.com/Tracker?data=ivPIaZ1M97sI-f2KN-08EdPH6mjSpiSN5KlK5_wlQbAAc4LWQocEKA9WUvb12WpwAN9k7iI4dL7FhQDxff_oY9qsBJJggCsRDLKBn9d-juCsq_E1nYXWUbPkipiFX7v6c5txgiRkYTmedLH_CMbGZGrwjGeppu4zTKTte98OnPG6O31YTGLfYCMEgU_q7Nda9e_0jwSblQw2MaRpdEflJOyNutWjOqPotKN5lxqDg-Y1UUF9H972qTWMlpwJdASFnH4jOkFTx4G1ePOUVApIr4lh_Q4tBul_A5aN9Go-704pV8GyzBO3XsQh6R2zmyotgeo7OJSsVJWiPMbdy8Xdpk0xIB81zv7DL1skxttlNuoVFX2_gQqD22FlIZX0eJTHeJ4_Im5HsRBZxO8iY08JPj9YO5W8wQjQbQGCEeCWAtJOzt79X-w9kpWvV30q2_Nv3_GHClF6m_ipTs6A3Dni9l8ihAggbB8JCtlahmKisZOERjyUz15eR5cyoeIbeX34hCzjvnsVJq2WYbfXyUWRcQ==">www.kuraoncology.com</a>&nbsp;and follow us on&nbsp;<a href="https://www.globenewswire.com/Tracker?data=0XrzPmD93VFEFgLaVr3RDXJ4YJ9GwVIrdBdEpaZqOXlWVFt2wNf-GaUGGD7vAJGfpHH18a0knFqQZ3VKcNbSrfyAweMLIwpkC8zrSNvFkBKLuOr_mnRS1Dq1TXP3--WW3ozJKzm5Tf2uvnAeJde-MlQBsDQieWSjNaw9g8uMPbWUxqjjWPc-YvQO5FjwEFspnPDZ7SsZ9Tj6xZxHPbhm0cG1woV_LAfBhUuAUorGYEwe1p023CEmpdHBqytB1Hb2Lca3QvrupWDzdPliVnBnazwblrZopi5a9BjP35irdevpYuevM0xDkPqhUbDaUOzsO8quAx--cMtliGWkIqyNO8BBXruqdidcb-dKXVzK9nnWNdBqNyJdnGJ_FKMNtSgvxpSjFm89EWwQk-2tCFVy-c3DiP3QOTNUsNZfdDvdalWiXA790TBE8-m6he3SH5kJE0jHosqjsWdQZ_LmmhF-APnsj5zLK30H9lJT_96t4y7taBZS9EgCbnKlIuMtg4Xt5QZ3XfY4a4QFzsKkZGcGZaOxBs148YXiBRrEMpHuVxm9Ed81NLoog4lyhe73Qdj3GJgvxI_UpHE9P2EWjVIO8wztEdDxd5kzg8Rbdp-HQ6fVkffcVZUaw1aYoJbRztrn9uzPu0qhXXcEooOlLAVcfA==">X</a>&nbsp;and&nbsp;<a href="https://www.globenewswire.com/Tracker?data=09ovKsXTlPV0n7MjNVrrRqAWBywJUeOxMzA_nYB0Mk0aAGczYB85764GV7bV1rte53dGawh5WyBhpHnXGI3ssuWm-1o-T3NalGIRz42ZpjYzyMPck9PFykD3kxqzRwUW5X1cNHoiCrfr5XfhWSBbdOWzC0i3dmxbxaPyBaKvqdJJIoR5mFg0YjYqYom9B-2uixJr1C2ZRKFqzkhKjPfkfPRiHu0QgJbQ8VPufnQc5Ac_860SJQLIG4kctJSyc1w4Ffp5NzgO0puLINW3Xsssd8lishssXKnQRc6IqzmMb3u1-FAJBoOauwh-pIEfxweaJy1Es3TEUOcN1aC0PFe8Cjp3IAkNSMq-1imazyxbc7QP4xj93QysOCLUdwT62O3Y4nP3TSl5cHBn2DIiUxW70gqQ04L2wUWgy14Tpl5CEYJ_Hp_JG3JIwh0SCWhbF7uPWoXfbcrK-jMjSsVM8JoNm7pt5tWA5e5m5iIFpNFP-Gn0zx9jrc3TinLD9ksPonmmf6uEP1loaxtKd5rIPeTu69E9mgnOePqMSIYZbKFuGtAmvd91F_7XiB7EuoN9SCHKhLkCCsx1L2X1ke2blh18xjL6t3jv11C5XEcAub-aF4mR74hLvWszpX-ExXnoUSZ_UBQiBNPy7DDNL04gHSnuqC2kOA5hR-na6ZUWrbrqtCgTtGNAhy5DpGJIOjsw0tU-hrD9rGbElmP7pbzVapAp9-SLXRbGbRnr2LtXtAH4rPc=">LinkedIn</a>.
Kura Oncology is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.&nbsp;
If you are a California resident, please see the attached Privacy Notice&nbsp;<a href="https://bit.ly/43vcIhg">CA Privacy Notice</a></div>

Associate Director, Medical & Regulatory Writing

<div class="content-intro">Are you ready to join a team committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines? At Kura Oncology, you have an opportunity to be a part of something bigger, with a lasting impact that you can be proud of.
At Kura Oncology, we are working to change the paradigm and improve the science of cancer treatment. As an organization, we strive to cultivate a diverse and talented professional culture driven to develop precision medicine therapeutics.
As we continue to build a leading biotech organization with a strong culture, a patient-focused mindset and a team focused on relentless execution, we are looking for innovative, passionate professionals to join us and make our vision a reality.
To succeed at Kura, you will need to have a demonstrated ability for excellence in drug discovery and development and a roll-up your sleeves attitude. The ideal candidate will possess a values-driven work style where integrity and grit drive all behaviors, decisions, and actions.</div>ESSENTIAL JOB FUNCTIONS:
We are seeking an experienced and visionary leader to join our IT leadership team as the Associate Director/Director of IT. This pivotal role reporting to the Head of IT, will be responsible for shaping and executing our IT strategy, managing our IT portfolio, driving change management initiatives, leading IT communications, refining our IT operating model, co-managing IT budget and forecasting and supporting business system owners (BSO’s) in new compliance initiatives
IT Strategy and Portfolio Management
<ul>
<li>Develop, implement, and continuously refine a comprehensive IT strategy&nbsp;in partnership with the Head of IT and functional stakeholders&nbsp;that aligns with and supports overall business objectives.</li>
<li>Drive innovation by integrating emerging technologies and leading digital transformation initiatives that align with the strategic vision of Kura Oncology.</li>
<li>Establish and maintain a robust IT portfolio management framework, including tools and processes for project prioritization, resource allocation, and performance tracking.</li>
<li>Conduct regular portfolio reviews to ensure optimal balance of risk, value, and strategic alignment.</li>
<li>Collaborate with business units and system owners to identify and prioritize IT initiatives that drive business value.</li>
<li>Implement and maintain security policies based on roadmap initiatives and business goals of the company.</li>
<li>Evaluate system vulnerabilities and conduct regular audits, risk assessments, and compliance checks to ensure security standards are met.</li>
<li>Coordinate with the Incident response team in responding to any security incidents and investigating root causes, while implementing corrective measures to prevent future occurrences.</li>
</ul>
AI Strategy, Governance, and Enablement
<ul>
<li>Partner with the Head of IT and business leaders to develop and execute the company’s enterprise AI strategy and roadmap, identifying opportunities to leverage artificial intelligence, generative AI, and automation to improve productivity, decision making, and business outcomes.</li>
<li>Establish and maintain an AI governance framework addressing appropriate use, data privacy, information security, regulatory compliance, intellectual property, risk management, and responsible AI practices.</li>
<li>Lead the evaluation, selection, and implementation of enterprise AI platforms, tools, and capabilities, ensuring alignment with the company’s technology architecture, security requirements, and business objectives.</li>
<li>Partner with functional stakeholders to identify, prioritize, and develop high value AI use cases across the organization, establishing clear business outcomes, ownership, success criteria, and measures of value.</li>
<li>Collaborate with Information Security, Legal, Compliance, Quality, and business stakeholders to assess and manage risks associated with AI technologies, including sensitive and confidential data, model outputs, third party services, and regulatory requirements.</li>
<li>Develop policies, standards, and procedures governing the responsible use of generative AI and other AI technologies across the organization.</li>
<li>Drive responsible adoption of AI through employee education, training, communications, and change management programs that improve AI literacy and encourage effective and appropriate use of approved AI tools.</li>
<li>Ensure AI solutions supporting GxP or other regulated business processes are appropriately assessed, documented, validated, and governed in partnership with Quality and applicable Business System Owners.</li>
</ul>
Change Management and Communications
<ul>
<li>Develop and execute comprehensive change management strategies for major IT initiatives and organizational transformations.</li>
<li>Create and maintain a change management framework&nbsp;and&nbsp;train IT Team on effective use to deliver change in a consistent manner.</li>
<li>Lead the development and execution of multi-channel IT communication plans, ensuring clear and effective messaging to all stakeholders.</li>
<li>Establish feedback mechanisms to measure the effectiveness of change initiatives and communications.</li>
<li>Collaborate with HR and other departments to align IT changes with broader organizational change efforts.</li>
</ul>
Compliance &amp; Validation Management
<ul>
<li>Ensure IT systems used in GxP-regulated processes and implemented, validated, and maintained according to regulatory standards and Kura business processes.</li>
<li>Collaborate with Business Systems Owners, IT, and Quality teams to develop and execute validation deliverables (IQ/OQ/PQ).</li>
<li>Monitor system changes to ensure compliance with change control procedures and regulatory standards</li>
</ul>
GxP System Audits and Inspections
<ul>
<li>Support internal and external audits, including those conducted by regulatory authorities (e.g., FDA, EMA).</li>
<li>Prepare compliance documentation and provide necessary evidence for GxP audits and inspections.</li>
<li>Follow up on audit findings and assist with remediation plans to close gaps</li>
</ul>
IT Operating Model and Governance
<ul>
<li>Continuously assess and refine the IT operating model to enhance efficiency, effectiveness, and alignment with business needs.</li>
<li>Establish and maintain IT governance frameworks, including decision-making processes&nbsp;to support cross functional steering committees and&nbsp;drive efficiencies&nbsp;across&nbsp;IT.</li>
<li>Develop and oversee IT performance metrics and scorecards to drive continuous improvement.</li>
</ul>
Budget and Forecasting
<ul>
<li>Working with Head of IT to oversee the development and management of the annual IT budget, ensuring alignment with strategic priorities&nbsp;and maximizing ROI on IT investments.</li>
<li>Implement robust financial management processes&nbsp;that can be quickly adopted/adapted to by the IT Team.</li>
<li>Develop accurate IT financial forecasts, considering technology trends and business growth projections.</li>
</ul>
JOB SPECIFICATIONS:
<ul>
<li>Bachelor’s degree in a related technical or business discipline required.</li>
<li>A minimum of 8-10 years of progressive experience in IT leadership roles, with at least 5 years in management positions</li>
<li>Proven track record in developing and implementing enterprise-wide IT strategies that drive business value</li>
<li>Understanding of current security practices and standards for mid-size enterprise IT</li>
<li>Extensive experience in portfolio management, including the use of portfolio management tools and methodologies</li>
<li>Strong background in change management, with demonstrated success in managing complex organizational changes</li>
<li>Expertise in IT financial management, including budgeting, forecasting, and cost optimization techniques, SOX reporting</li>
<li>In-depth knowledge of IT governance frameworks (e.g., COBIT, ITIL) and experience implementing governance structures</li>
<li>Proven ability to communicate effectively with C-level executives, board members, and diverse stakeholder groups</li>
<li>Strong analytical skills with the ability to translate complex technical concepts into business terms</li>
<li>Experience with digital transformation initiatives and emerging technologies (e.g., cloud, AI, IoT)</li>
<li>Track record of building and leading high-performing teams in a fast-paced, dynamic environment</li>
<li>Strong negotiation skills and experience managing vendor relationships and contracts</li>
<li>Demonstrated commitment to continuous learning and staying current with industry trends and best practices</li>
<li>Makes decisions for assigned programs or functional areas, balancing priorities and resolving routine challenges; escalates high-impact or cross-functional decisions as needed.</li>
<li>Facilitates cross-functional coordination for assigned programs or initiatives, ensuring alignment and timely execution of deliverables.</li>
</ul>
The base range for this role at the Associate Director level is $186,000 - $218,000 and Director level is $221,000 - $259,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location, and relevant education or training. Kura's compensation package also includes generous benefits, equity, and participation in an annual target bonus.
#LI-RM1
&nbsp;
&nbsp;<div class="content-conclusion">Kura’s Values that are used for candidate selection and performance assessments:
<ul>
<li>We work as one for patients</li>
<li>We are goal-focused and deliver with excellence</li>
<li>We are science-driven courageous innovators</li>
<li>We strive to bring out the best in each other and ourselves</li>
</ul>
The Kura Package 
<ul>
<li>Career advancement/ development opportunities</li>
<li>Competitive comp package</li>
<li>Bonus</li>
<li>401K + Employer contributions</li>
<li>Generous stock options</li>
<li>ESPP Plan</li>
<li>20 days of PTO to start</li>
<li>18 Holidays&nbsp; (Including Summer &amp; Winter Break)</li>
<li>Generous Benefits Package with a variety of plans available with a substantial employer match</li>
<li>Paid Paternity/Maternity Leave</li>
<li>In-Office Catered lunches</li>
<li>Home Office Setup</li>
<li>Lifestyle Spending Stipend</li>
<li>Commuter Stipend (Boston Office)</li>
<li>Regular employee social activities, including happy hours, monthly birthday celebrations, Kura Koffee Talks, and much more!</li>
</ul>
Kura Oncology is a commercial-stage biopharmaceutical company committed to discovering and developing innovative precision medicines to help patients with cancer lead better, longer lives.
Through our deep understanding of cancer biology and decades of experience in precision oncology, we are studying the underlying causes of treatment resistance. This enables us to design smart combination regimens with other cancer therapies to target tumors from multiple directions, with the goal of improving long-term clinical benefit.
Kura developed and is commercializing KOMZIFTI® (ziftomenib), the FDA-approved once-daily, oral menin inhibitor for the treatment of adults with relapsed or refractory NPM1-mutated acute myeloid leukemia, and continues to pioneer advancements in menin inhibition and farnesyl transferase inhibition. For additional information, please visit Kura’s website at&nbsp;<a href="https://www.globenewswire.com/Tracker?data=ivPIaZ1M97sI-f2KN-08EdPH6mjSpiSN5KlK5_wlQbAAc4LWQocEKA9WUvb12WpwAN9k7iI4dL7FhQDxff_oY9qsBJJggCsRDLKBn9d-juCsq_E1nYXWUbPkipiFX7v6c5txgiRkYTmedLH_CMbGZGrwjGeppu4zTKTte98OnPG6O31YTGLfYCMEgU_q7Nda9e_0jwSblQw2MaRpdEflJOyNutWjOqPotKN5lxqDg-Y1UUF9H972qTWMlpwJdASFnH4jOkFTx4G1ePOUVApIr4lh_Q4tBul_A5aN9Go-704pV8GyzBO3XsQh6R2zmyotgeo7OJSsVJWiPMbdy8Xdpk0xIB81zv7DL1skxttlNuoVFX2_gQqD22FlIZX0eJTHeJ4_Im5HsRBZxO8iY08JPj9YO5W8wQjQbQGCEeCWAtJOzt79X-w9kpWvV30q2_Nv3_GHClF6m_ipTs6A3Dni9l8ihAggbB8JCtlahmKisZOERjyUz15eR5cyoeIbeX34hCzjvnsVJq2WYbfXyUWRcQ==">www.kuraoncology.com</a>&nbsp;and follow us on&nbsp;<a href="https://www.globenewswire.com/Tracker?data=0XrzPmD93VFEFgLaVr3RDXJ4YJ9GwVIrdBdEpaZqOXlWVFt2wNf-GaUGGD7vAJGfpHH18a0knFqQZ3VKcNbSrfyAweMLIwpkC8zrSNvFkBKLuOr_mnRS1Dq1TXP3--WW3ozJKzm5Tf2uvnAeJde-MlQBsDQieWSjNaw9g8uMPbWUxqjjWPc-YvQO5FjwEFspnPDZ7SsZ9Tj6xZxHPbhm0cG1woV_LAfBhUuAUorGYEwe1p023CEmpdHBqytB1Hb2Lca3QvrupWDzdPliVnBnazwblrZopi5a9BjP35irdevpYuevM0xDkPqhUbDaUOzsO8quAx--cMtliGWkIqyNO8BBXruqdidcb-dKXVzK9nnWNdBqNyJdnGJ_FKMNtSgvxpSjFm89EWwQk-2tCFVy-c3DiP3QOTNUsNZfdDvdalWiXA790TBE8-m6he3SH5kJE0jHosqjsWdQZ_LmmhF-APnsj5zLK30H9lJT_96t4y7taBZS9EgCbnKlIuMtg4Xt5QZ3XfY4a4QFzsKkZGcGZaOxBs148YXiBRrEMpHuVxm9Ed81NLoog4lyhe73Qdj3GJgvxI_UpHE9P2EWjVIO8wztEdDxd5kzg8Rbdp-HQ6fVkffcVZUaw1aYoJbRztrn9uzPu0qhXXcEooOlLAVcfA==">X</a>&nbsp;and&nbsp;<a href="https://www.globenewswire.com/Tracker?data=09ovKsXTlPV0n7MjNVrrRqAWBywJUeOxMzA_nYB0Mk0aAGczYB85764GV7bV1rte53dGawh5WyBhpHnXGI3ssuWm-1o-T3NalGIRz42ZpjYzyMPck9PFykD3kxqzRwUW5X1cNHoiCrfr5XfhWSBbdOWzC0i3dmxbxaPyBaKvqdJJIoR5mFg0YjYqYom9B-2uixJr1C2ZRKFqzkhKjPfkfPRiHu0QgJbQ8VPufnQc5Ac_860SJQLIG4kctJSyc1w4Ffp5NzgO0puLINW3Xsssd8lishssXKnQRc6IqzmMb3u1-FAJBoOauwh-pIEfxweaJy1Es3TEUOcN1aC0PFe8Cjp3IAkNSMq-1imazyxbc7QP4xj93QysOCLUdwT62O3Y4nP3TSl5cHBn2DIiUxW70gqQ04L2wUWgy14Tpl5CEYJ_Hp_JG3JIwh0SCWhbF7uPWoXfbcrK-jMjSsVM8JoNm7pt5tWA5e5m5iIFpNFP-Gn0zx9jrc3TinLD9ksPonmmf6uEP1loaxtKd5rIPeTu69E9mgnOePqMSIYZbKFuGtAmvd91F_7XiB7EuoN9SCHKhLkCCsx1L2X1ke2blh18xjL6t3jv11C5XEcAub-aF4mR74hLvWszpX-ExXnoUSZ_UBQiBNPy7DDNL04gHSnuqC2kOA5hR-na6ZUWrbrqtCgTtGNAhy5DpGJIOjsw0tU-hrD9rGbElmP7pbzVapAp9-SLXRbGbRnr2LtXtAH4rPc=">LinkedIn</a>.
Kura Oncology is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.&nbsp;
If you are a California resident, please see the attached Privacy Notice&nbsp;<a href="https://bit.ly/43vcIhg">CA Privacy Notice</a></div>

Assoc Director/Director, IT

<div class="content-intro">Are you ready to join a team committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines? At Kura Oncology, you have an opportunity to be a part of something bigger, with a lasting impact that you can be proud of.
At Kura Oncology, we are working to change the paradigm and improve the science of cancer treatment. As an organization, we strive to cultivate a diverse and talented professional culture driven to develop precision medicine therapeutics.
As we continue to build a leading biotech organization with a strong culture, a patient-focused mindset and a team focused on relentless execution, we are looking for innovative, passionate professionals to join us and make our vision a reality.
To succeed at Kura, you will need to have a demonstrated ability for excellence in drug discovery and development and a roll-up your sleeves attitude. The ideal candidate will possess a values-driven work style where integrity and grit drive all behaviors, decisions, and actions.</div><h2>ESSENTIAL JOB FUNCTIONS</h2>
The Senior Executive Assistant, Commercial is a highly trusted partner responsible for providing exceptional support to the Chief Commercial Officer (CCO) and broader Commercial Leadership Team. This individual helps maximize leadership effectiveness through strong organization, judgment, discretion, and proactive coordination across the Commercial organization.
The successful candidate anticipates needs, manages competing priorities, facilitates communication and follow-through, and helps ensure leaders remain focused on the priorities that have the greatest impact on the business.
This individual is highly resourceful, technologically savvy, and comfortable leveraging technology, AI, and emerging tools to improve productivity and ways of working.
<ul>
<li>Provide high-level executive support to the Chief Commercial Officer and administrative and coordination support to members of the Commercial Leadership Team.</li>
<li>Strategically manage the CCO's complex and dynamic calendar, anticipating priorities, conflicts, preparation needs, and follow-up.</li>
<li>Coordinate calendars and scheduling across Commercial leadership to facilitate effective decision-making, collaboration, and execution.</li>
<li>Coordinate complex domestic and international travel, itineraries, logistics, and expenses for the CCO and Commercial leaders as needed.</li>
<li>Plan and coordinate Commercial Leadership Team meetings, offsites, conferences, team meetings, and key Commercial events.</li>
<li>Prepare meeting agendas, briefing materials, presentations, and other communications; ensure decisions, commitments, and action items are captured and tracked to completion.</li>
<li>Help establish and maintain effective operating rhythms across the Commercial Leadership Team, including recurring meetings, planning activities, and key milestones.</li>
<li>Identify and adopt technology, including appropriate AI-enabled tools and automation, to improve executive and Commercial team efficiency.</li>
<li>Proactively identify scheduling conflicts, competing priorities, and potential obstacles and take appropriate action to resolve them.</li>
<li>Support selected Commercial projects and initiatives, coordinating stakeholders, timelines, logistics, and deliverables as appropriate.</li>
<li>Coordinate contracts, purchase orders, expenses, and other administrative processes in partnership with internal functions.</li>
<li>Manage sensitive and confidential business and personnel information with exceptional discretion and sound judgment.</li>
<li>Build strong relationships across Commercial, other functions, and the administrative team to enable effective collaboration and execution.</li>
</ul>
<h2>JOB SPECIFICATIONS:</h2>
<ul>
<li>Bachelor's degree preferred or equivalent combination of education and relevant experience.</li>
<li>8+ years of executive administrative experience, including experience supporting senior executives; biotech/pharmaceutical industry experience strongly preferred.</li>
<li>Ability to be onsite in the San Diego office 2-3 times per week</li>
<li>Exceptional organizational, project management, communication, and problem-solving skills.</li>
<li>Demonstrated ability to anticipate needs, manage multiple priorities, and operate independently in a fast-paced, changing environment.</li>
<li>Excellent judgment, discretion, emotional intelligence, professionalism, and relationship-building skills.</li>
<li>Strong technological fluency with demonstrated curiosity and aptitude for adopting AI and emerging productivity tools.</li>
<li>Resourceful, proactive, detail-oriented, and committed to delivering with excellence.</li>
<li>Ability to work flexibly across time zones and changing priorities.</li>
</ul>
WHAT EXCELLENCE LOOKS LIKE:
The exceptional Senior Executive Assistant creates executive leverage. They anticipate what the CCO and Commercial Leadership Team need, surface issues early, close open loops, and create organization and structure that allow leaders to operate more effectively.
They are proactive, highly resourceful, and continually look for smarter ways to work; including thoughtful use of technology, AI, and automation.
Success means the CCO and Commercial leaders are prepared, connected, organized, and able to spend their time on the work that creates the greatest value for patients and the Company.
The base range for a Senior Executive EA is $124,000 - $155,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location, and relevant education or training. Kura's compensation package also includes generous benefits, equity, and participation in an annual target bonus.
#LI-RM1<div class="content-conclusion">Kura’s Values that are used for candidate selection and performance assessments:
<ul>
<li>We work as one for patients</li>
<li>We are goal-focused and deliver with excellence</li>
<li>We are science-driven courageous innovators</li>
<li>We strive to bring out the best in each other and ourselves</li>
</ul>
The Kura Package 
<ul>
<li>Career advancement/ development opportunities</li>
<li>Competitive comp package</li>
<li>Bonus</li>
<li>401K + Employer contributions</li>
<li>Generous stock options</li>
<li>ESPP Plan</li>
<li>20 days of PTO to start</li>
<li>18 Holidays&nbsp; (Including Summer &amp; Winter Break)</li>
<li>Generous Benefits Package with a variety of plans available with a substantial employer match</li>
<li>Paid Paternity/Maternity Leave</li>
<li>In-Office Catered lunches</li>
<li>Home Office Setup</li>
<li>Lifestyle Spending Stipend</li>
<li>Commuter Stipend (Boston Office)</li>
<li>Regular employee social activities, including happy hours, monthly birthday celebrations, Kura Koffee Talks, and much more!</li>
</ul>
Kura Oncology is a commercial-stage biopharmaceutical company committed to discovering and developing innovative precision medicines to help patients with cancer lead better, longer lives.
Through our deep understanding of cancer biology and decades of experience in precision oncology, we are studying the underlying causes of treatment resistance. This enables us to design smart combination regimens with other cancer therapies to target tumors from multiple directions, with the goal of improving long-term clinical benefit.
Kura developed and is commercializing KOMZIFTI® (ziftomenib), the FDA-approved once-daily, oral menin inhibitor for the treatment of adults with relapsed or refractory NPM1-mutated acute myeloid leukemia, and continues to pioneer advancements in menin inhibition and farnesyl transferase inhibition. For additional information, please visit Kura’s website at&nbsp;<a href="https://www.globenewswire.com/Tracker?data=ivPIaZ1M97sI-f2KN-08EdPH6mjSpiSN5KlK5_wlQbAAc4LWQocEKA9WUvb12WpwAN9k7iI4dL7FhQDxff_oY9qsBJJggCsRDLKBn9d-juCsq_E1nYXWUbPkipiFX7v6c5txgiRkYTmedLH_CMbGZGrwjGeppu4zTKTte98OnPG6O31YTGLfYCMEgU_q7Nda9e_0jwSblQw2MaRpdEflJOyNutWjOqPotKN5lxqDg-Y1UUF9H972qTWMlpwJdASFnH4jOkFTx4G1ePOUVApIr4lh_Q4tBul_A5aN9Go-704pV8GyzBO3XsQh6R2zmyotgeo7OJSsVJWiPMbdy8Xdpk0xIB81zv7DL1skxttlNuoVFX2_gQqD22FlIZX0eJTHeJ4_Im5HsRBZxO8iY08JPj9YO5W8wQjQbQGCEeCWAtJOzt79X-w9kpWvV30q2_Nv3_GHClF6m_ipTs6A3Dni9l8ihAggbB8JCtlahmKisZOERjyUz15eR5cyoeIbeX34hCzjvnsVJq2WYbfXyUWRcQ==">www.kuraoncology.com</a>&nbsp;and follow us on&nbsp;<a href="https://www.globenewswire.com/Tracker?data=0XrzPmD93VFEFgLaVr3RDXJ4YJ9GwVIrdBdEpaZqOXlWVFt2wNf-GaUGGD7vAJGfpHH18a0knFqQZ3VKcNbSrfyAweMLIwpkC8zrSNvFkBKLuOr_mnRS1Dq1TXP3--WW3ozJKzm5Tf2uvnAeJde-MlQBsDQieWSjNaw9g8uMPbWUxqjjWPc-YvQO5FjwEFspnPDZ7SsZ9Tj6xZxHPbhm0cG1woV_LAfBhUuAUorGYEwe1p023CEmpdHBqytB1Hb2Lca3QvrupWDzdPliVnBnazwblrZopi5a9BjP35irdevpYuevM0xDkPqhUbDaUOzsO8quAx--cMtliGWkIqyNO8BBXruqdidcb-dKXVzK9nnWNdBqNyJdnGJ_FKMNtSgvxpSjFm89EWwQk-2tCFVy-c3DiP3QOTNUsNZfdDvdalWiXA790TBE8-m6he3SH5kJE0jHosqjsWdQZ_LmmhF-APnsj5zLK30H9lJT_96t4y7taBZS9EgCbnKlIuMtg4Xt5QZ3XfY4a4QFzsKkZGcGZaOxBs148YXiBRrEMpHuVxm9Ed81NLoog4lyhe73Qdj3GJgvxI_UpHE9P2EWjVIO8wztEdDxd5kzg8Rbdp-HQ6fVkffcVZUaw1aYoJbRztrn9uzPu0qhXXcEooOlLAVcfA==">X</a>&nbsp;and&nbsp;<a href="https://www.globenewswire.com/Tracker?data=09ovKsXTlPV0n7MjNVrrRqAWBywJUeOxMzA_nYB0Mk0aAGczYB85764GV7bV1rte53dGawh5WyBhpHnXGI3ssuWm-1o-T3NalGIRz42ZpjYzyMPck9PFykD3kxqzRwUW5X1cNHoiCrfr5XfhWSBbdOWzC0i3dmxbxaPyBaKvqdJJIoR5mFg0YjYqYom9B-2uixJr1C2ZRKFqzkhKjPfkfPRiHu0QgJbQ8VPufnQc5Ac_860SJQLIG4kctJSyc1w4Ffp5NzgO0puLINW3Xsssd8lishssXKnQRc6IqzmMb3u1-FAJBoOauwh-pIEfxweaJy1Es3TEUOcN1aC0PFe8Cjp3IAkNSMq-1imazyxbc7QP4xj93QysOCLUdwT62O3Y4nP3TSl5cHBn2DIiUxW70gqQ04L2wUWgy14Tpl5CEYJ_Hp_JG3JIwh0SCWhbF7uPWoXfbcrK-jMjSsVM8JoNm7pt5tWA5e5m5iIFpNFP-Gn0zx9jrc3TinLD9ksPonmmf6uEP1loaxtKd5rIPeTu69E9mgnOePqMSIYZbKFuGtAmvd91F_7XiB7EuoN9SCHKhLkCCsx1L2X1ke2blh18xjL6t3jv11C5XEcAub-aF4mR74hLvWszpX-ExXnoUSZ_UBQiBNPy7DDNL04gHSnuqC2kOA5hR-na6ZUWrbrqtCgTtGNAhy5DpGJIOjsw0tU-hrD9rGbElmP7pbzVapAp9-SLXRbGbRnr2LtXtAH4rPc=">LinkedIn</a>.
Kura Oncology is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.&nbsp;
If you are a California resident, please see the attached Privacy Notice&nbsp;<a href="https://bit.ly/43vcIhg">CA Privacy Notice</a></div>

Senior Executive Assistant, Commercial

<div class="content-intro">Are you ready to join a team committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines? At Kura Oncology, you have an opportunity to be a part of something bigger, with a lasting impact that you can be proud of.
At Kura Oncology, we are working to change the paradigm and improve the science of cancer treatment. As an organization, we strive to cultivate a diverse and talented professional culture driven to develop precision medicine therapeutics.
As we continue to build a leading biotech organization with a strong culture, a patient-focused mindset and a team focused on relentless execution, we are looking for innovative, passionate professionals to join us and make our vision a reality.
To succeed at Kura, you will need to have a demonstrated ability for excellence in drug discovery and development and a roll-up your sleeves attitude. The ideal candidate will possess a values-driven work style where integrity and grit drive all behaviors, decisions, and actions.</div>ESSENTIAL JOB FUNCTIONS:
The Senior Director of Alliance Management will play a critical role in managing and optimizing Kura’s strategic alliance with Kyowa Kirin, supporting the strategic and operational execution of our programs. This individual will be responsible for leading and overseeing the management of strategic partnerships including governance, developing and executing alliance strategies, fostering collaboration and communication between internal teams and external partners, and ensuring that partnerships delivery mutual value.
The successful candidate will combine strategic thinking with a strong bias for action; be able to anticipate issues, frame complex decisions, plan and drive governance interactions, and provide thoughtful recommendations, while also taking ownership for translating those recommendations into clear actions and results. This role requires a confident and credible leader who is willing to raise and address difficult issues, constructively challenge internal and external stakeholders when needed, and hold both internal teams and external partners accountable to agreed-upon commitments
<ul>
<li>Develop and execute the overall alliance management strategy aligned with the organization’s business objectives, partnership agreements, and long-term strategic priorities.</li>
<li>Build and maintain strong, trusted relationships with Joint Committee members, alliance governance leaders, internal stakeholders, and external partner counterparts to enable candid dialogue, effective decision-making, and productive collaboration.</li>
<li>Facilitate and coordinate joint committees and working groups to promote collaboration among partners.</li>
<li>Drive accountability to the partnership agreement and governance decisions, ensuring that commitments, obligations, milestones, and agreed-upon actions are understood and fulfilled by both internal teams and external partners.&nbsp;</li>
<li>Serve as the primary point of contact for partners, maintaining strong relationships and clear communication.</li>
<li>Drive continuous improvement to strengthen the partnership to support program execution aligned to the partnership agreements</li>
<li>Partner with Program Leadership and Program Management to translate strategic discussions and governance decisions into clear execution plans, owners, timelines and deliverables, and own follow-through across internal partner teams.</li>
<li>Establish communication and decision-making protocols among alliance teams and with the partner; ensures contractually required communication occurs in a timely manner.</li>
<li>Accurately interpret contracts and manages contractual obligations; establish and monitor metrics and milestones; negotiate amendments to contracts; and manage conflict resolutions and escalation when necessary.</li>
</ul>
JOB SPECIFICATIONS:
<ul>
<li>Advanced degree in life sciences, business administration, or a related field is preferred.</li>
<li>Significant experience in alliance management or partnership development and commercialization within the pharmaceutical biotechnology industry.</li>
<li>A minimum of 12 years experience.</li>
<li>Strong negotiation and communication skills, with the ability to manage complex relationships.</li>
<li>Strong executive presence and communications skills, with the confidence and judgement to raise difficult issues, constructively challenge stakeholders, and influence decisions across organizational boundaries.</li>
<li>Strategic thinking and problem-solving abilities, with a focus on achieving mutual goals.</li>
<li>Expertise in working within matrix teams, including cross-cultural teams and influencing without authority.</li>
<li>Experience working with a broad range of functions including commercial, business development, clinical development, CMC, R&amp;D, finance and legal.</li>
<li>Leads decision-making across multiple programs or areas, setting direction and making strategic trade-offs that impact cross-functional execution and outcomes.</li>
<li>Drives cross-functional alignment across multiple programs, influencing stakeholders to shape strategy and ensure cohesive execution across functions.</li>
</ul>
The base range for a Senior Director is $284,000 - $328,000 per year. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location, and relevant education or training. Kura's compensation package also includes generous benefits, equity, and participation in an annual target bonus.
#LI-RM1<div class="content-conclusion">Kura’s Values that are used for candidate selection and performance assessments:
<ul>
<li>We work as one for patients</li>
<li>We are goal-focused and deliver with excellence</li>
<li>We are science-driven courageous innovators</li>
<li>We strive to bring out the best in each other and ourselves</li>
</ul>
The Kura Package 
<ul>
<li>Career advancement/ development opportunities</li>
<li>Competitive comp package</li>
<li>Bonus</li>
<li>401K + Employer contributions</li>
<li>Generous stock options</li>
<li>ESPP Plan</li>
<li>20 days of PTO to start</li>
<li>18 Holidays&nbsp; (Including Summer &amp; Winter Break)</li>
<li>Generous Benefits Package with a variety of plans available with a substantial employer match</li>
<li>Paid Paternity/Maternity Leave</li>
<li>In-Office Catered lunches</li>
<li>Home Office Setup</li>
<li>Lifestyle Spending Stipend</li>
<li>Commuter Stipend (Boston Office)</li>
<li>Regular employee social activities, including happy hours, monthly birthday celebrations, Kura Koffee Talks, and much more!</li>
</ul>
Kura Oncology is a commercial-stage biopharmaceutical company committed to discovering and developing innovative precision medicines to help patients with cancer lead better, longer lives.
Through our deep understanding of cancer biology and decades of experience in precision oncology, we are studying the underlying causes of treatment resistance. This enables us to design smart combination regimens with other cancer therapies to target tumors from multiple directions, with the goal of improving long-term clinical benefit.
Kura developed and is commercializing KOMZIFTI® (ziftomenib), the FDA-approved once-daily, oral menin inhibitor for the treatment of adults with relapsed or refractory NPM1-mutated acute myeloid leukemia, and continues to pioneer advancements in menin inhibition and farnesyl transferase inhibition. For additional information, please visit Kura’s website at&nbsp;<a href="https://www.globenewswire.com/Tracker?data=ivPIaZ1M97sI-f2KN-08EdPH6mjSpiSN5KlK5_wlQbAAc4LWQocEKA9WUvb12WpwAN9k7iI4dL7FhQDxff_oY9qsBJJggCsRDLKBn9d-juCsq_E1nYXWUbPkipiFX7v6c5txgiRkYTmedLH_CMbGZGrwjGeppu4zTKTte98OnPG6O31YTGLfYCMEgU_q7Nda9e_0jwSblQw2MaRpdEflJOyNutWjOqPotKN5lxqDg-Y1UUF9H972qTWMlpwJdASFnH4jOkFTx4G1ePOUVApIr4lh_Q4tBul_A5aN9Go-704pV8GyzBO3XsQh6R2zmyotgeo7OJSsVJWiPMbdy8Xdpk0xIB81zv7DL1skxttlNuoVFX2_gQqD22FlIZX0eJTHeJ4_Im5HsRBZxO8iY08JPj9YO5W8wQjQbQGCEeCWAtJOzt79X-w9kpWvV30q2_Nv3_GHClF6m_ipTs6A3Dni9l8ihAggbB8JCtlahmKisZOERjyUz15eR5cyoeIbeX34hCzjvnsVJq2WYbfXyUWRcQ==">www.kuraoncology.com</a>&nbsp;and follow us on&nbsp;<a href="https://www.globenewswire.com/Tracker?data=0XrzPmD93VFEFgLaVr3RDXJ4YJ9GwVIrdBdEpaZqOXlWVFt2wNf-GaUGGD7vAJGfpHH18a0knFqQZ3VKcNbSrfyAweMLIwpkC8zrSNvFkBKLuOr_mnRS1Dq1TXP3--WW3ozJKzm5Tf2uvnAeJde-MlQBsDQieWSjNaw9g8uMPbWUxqjjWPc-YvQO5FjwEFspnPDZ7SsZ9Tj6xZxHPbhm0cG1woV_LAfBhUuAUorGYEwe1p023CEmpdHBqytB1Hb2Lca3QvrupWDzdPliVnBnazwblrZopi5a9BjP35irdevpYuevM0xDkPqhUbDaUOzsO8quAx--cMtliGWkIqyNO8BBXruqdidcb-dKXVzK9nnWNdBqNyJdnGJ_FKMNtSgvxpSjFm89EWwQk-2tCFVy-c3DiP3QOTNUsNZfdDvdalWiXA790TBE8-m6he3SH5kJE0jHosqjsWdQZ_LmmhF-APnsj5zLK30H9lJT_96t4y7taBZS9EgCbnKlIuMtg4Xt5QZ3XfY4a4QFzsKkZGcGZaOxBs148YXiBRrEMpHuVxm9Ed81NLoog4lyhe73Qdj3GJgvxI_UpHE9P2EWjVIO8wztEdDxd5kzg8Rbdp-HQ6fVkffcVZUaw1aYoJbRztrn9uzPu0qhXXcEooOlLAVcfA==">X</a>&nbsp;and&nbsp;<a href="https://www.globenewswire.com/Tracker?data=09ovKsXTlPV0n7MjNVrrRqAWBywJUeOxMzA_nYB0Mk0aAGczYB85764GV7bV1rte53dGawh5WyBhpHnXGI3ssuWm-1o-T3NalGIRz42ZpjYzyMPck9PFykD3kxqzRwUW5X1cNHoiCrfr5XfhWSBbdOWzC0i3dmxbxaPyBaKvqdJJIoR5mFg0YjYqYom9B-2uixJr1C2ZRKFqzkhKjPfkfPRiHu0QgJbQ8VPufnQc5Ac_860SJQLIG4kctJSyc1w4Ffp5NzgO0puLINW3Xsssd8lishssXKnQRc6IqzmMb3u1-FAJBoOauwh-pIEfxweaJy1Es3TEUOcN1aC0PFe8Cjp3IAkNSMq-1imazyxbc7QP4xj93QysOCLUdwT62O3Y4nP3TSl5cHBn2DIiUxW70gqQ04L2wUWgy14Tpl5CEYJ_Hp_JG3JIwh0SCWhbF7uPWoXfbcrK-jMjSsVM8JoNm7pt5tWA5e5m5iIFpNFP-Gn0zx9jrc3TinLD9ksPonmmf6uEP1loaxtKd5rIPeTu69E9mgnOePqMSIYZbKFuGtAmvd91F_7XiB7EuoN9SCHKhLkCCsx1L2X1ke2blh18xjL6t3jv11C5XEcAub-aF4mR74hLvWszpX-ExXnoUSZ_UBQiBNPy7DDNL04gHSnuqC2kOA5hR-na6ZUWrbrqtCgTtGNAhy5DpGJIOjsw0tU-hrD9rGbElmP7pbzVapAp9-SLXRbGbRnr2LtXtAH4rPc=">LinkedIn</a>.
Kura Oncology is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.&nbsp;
If you are a California resident, please see the attached Privacy Notice&nbsp;<a href="https://bit.ly/43vcIhg">CA Privacy Notice</a></div>

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