Nuvalent

Director, Medical Affairs Strategy

Nuvalent$230K — $260K *
US-AnywhereRemote in Cambridge, MA
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Advanced medical/scientific doctoral-level degree required (PharmD, PhD, MD, or equivalent)
  • 10+ years of experience in pharmaceutical/biotech industries; 3+ years in Medical Affairs preferred
  • Experience with contributing to medical strategy and strong operational skills
  • Oncology experience required; solid tumor experience strongly preferred
  • Prior experience with advisory boards, PRC/MRC, and ISR programs
  • Collaboration experience across Clinical and Commercial functions
  • Strong project management and scientific communication skills

Responsibilities

  • Support the development and execution of annual Medical Affairs plans
  • Collaborate with Clinical, Commercial, Regulatory, and Field Medical teams for strategic alignment
  • Manage Medical Affairs activities including advisory boards and scientific congress planning
  • Contribute to the Promotional Review Committee (PRC) and Medical Review Committee (MRC) for scientific accuracy
  • Support the planning and implementation of the Investigator-Sponsored Research (ISR) program
  • Integrate healthcare provider insights with Clinical Development for clinical trial design
  • Assist in developing internal Medical Affairs processes and guidance documents

Benefits

  • Medical, dental, and vision insurance
  • 401(k) retirement savings plan
  • Generous paid time off including summer and winter company shutdowns
  • Comprehensive benefits package to support employee financial and health well-being
Full Job Description
The Role:
Reporting to the Senior Director of Medical Affairs, the Associate Director, Medical Strategy will support the development and execution of Medical Affairs strategy. This role will contribute to cross-functional planning and implementation of medical initiatives, including advisory boards, evidence generation, investigator-sponsored research (ISR), and promotional/medical material review. The Associate Director will collaborate closely with Clinical Development, Commercial, Regulatory, and Field Medical teams to ensure strategic alignment and seamless execution.

Responsibilities:
• Support development and execution of annual Medical Affairs strategic and tactical plans.
• Collaborate cross-functionally with Clinical, Commercial, Regulatory, and Field Medical to ensure alignment with scientific and business objectives.
• Operationalize and manage Medical Affairs activities such as advisory boards, symposia, scientific congress planning, and educational initiatives.
• Serve as a key Medical Affairs contributor on the Promotional Review Committee (PRC) and Medical Review Committee (MRC) to ensure scientific accuracy, compliance, and alignment with medical strategy.
• Support the planning and implementation of the Investigator-Sponsored Research (ISR) program, including proposal review, coordination of internal evaluations, and communication with investigators.
• Partner with Clinical Development to integrate healthcare provider insights and support the design and execution of clinical trials.
• Collaborate with Commercial colleagues on compliant alignment of strategy and assist with development of promotional materials including slide decks, FAQs, and internal training content.
• Help develop and maintain internal Medical Affairs processes, SOPs, and guidance documents.
• Gather, synthesize, and share scientific and clinical insights from KOL interactions, advisory boards, and scientific conferences.
• Assist in vendor oversight and budget management for assigned initiatives.

Competencies Include:
• Demonstrated ability to collaborate across matrixed, cross-functional teams in a fast-paced environment.
• Proven ability to manage multiple projects simultaneously with attention to timelines and detail.
• Strong communication and interpersonal skills; build trust and foster relationships internally and externally.
• Able to work independently, take initiative, and adapt quickly to evolving priorities.
• Recognized leader who exhibits effective communication, emotional intelligence, and influencing skills, within a matrix operating environment.
• Demonstration of strategic thinking and high-level planning while also balancing the ability to manage and execute operational details.
• Ability to effectively manage multiple projects with competing priorities.

Qualifications:
• Advanced, medical/scientific doctoral-level degree required: PharmD, PhD, MD (or equivalent).
• 10 + years of experience in the pharmaceutical biotech or other relevant industries, including 3+ years in Medical Affairs is preferred
• Experience contributing to medical strategy with strong operational and executional skills.
• Oncology experience required; solid tumor experience strongly preferred.
• Prior experience supporting advisory boards, PRC/MRC, and ISR programs.
• Experience collaborating across Clinical and Commercial functions.
• Strong project management and scientific communication skills.
• Up to 25% domestic (and possibly international) travel

Annual Salary Range

$230,000-$260,000 USD

Additional Information:

Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with competitive total rewards packages.

The targeted salary range reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors. The range will be reviewed regularly and is subject to change.

Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401(k) retirement savings plan, generous paid time off (including a summer and winter company shutdown), and much more.

About Nuvalent

Nuvalent is a biotechnology company that is focused on developing small molecule kinase inhibitors for cancer treatment. The company's lead product candidate, NUV-520, is a potent and selective inhibitor of the ERK kinase pathway, which is frequently dysregulated in cancer. Nuvalent is also developing a pipeline of other kinase inhibitors for the treatment of various cancers. The company was founded in 2019 and is headquartered in Pittsburgh, Pennsylvania.
Learn more about Nuvalent
Size
20 employees
Market Cap
$1.5 billion
Industry
NASDAQ

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