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Director, Medical Affairs Strategy

  • Nuvalent, Inc.

    • Remote
    • Massachusetts

Senior Oncology Account Manager (Sales)

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    • Remote
    • Virginia

Senior Precision Engagement Manager (US Sales): Southeast

  • Nuvalent, Inc.

    • Remote
    • Alabama
    • Washington DC
    • Delaware
    • Florida

Senior Regional Business Director (US Sales): Southeast

  • Nuvalent, Inc.

    • Remote
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    • Maryland
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Director, Medical Affairs Strategy

  • Nuvalent, Inc.

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Remote

Not Disclosed

Bio-Pharma

Marketing+1

  • Posted on:

Job Description

Summary

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.
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
Experience:

10-15 yrs

  • Skills:
  • Medical Affairs Strategy & Tactical Planning
  • Oncology / Solid Tumor Medical Affairs
  • Advisory Board & KOL Engagement
  • Investigator-Sponsored Research
  • Promotional & Medical Material Review — PRC/MRC
  • Clinical Development & Evidence Generation
  • Job Type:
  • Full-time
  • Shift Type:
  • 8 hour shift
  • Monday to Friday
  • Day shift

Compensation

  • Benefits:
  • 401K
  • 401K Match
  • Medical, Dental, Vision
  • Additional:
  • Base Salary

Job ID:

CGXP_26_15853

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