Jobs · Management

Senior Director, Medical Affairs

Inventiva Pharma · United States · 2 wk ago
RemoteRemoteManagementFull-time

About the role

We are seeking an experienced and strategic Senior Director, Medical Affairs to drive U.S. medical affairs activities during a critical transition from late-stage development to launch readiness. This is a highly visible role with significant impact on how our Phase 3 data are interpreted, communicated, and translated into clinical and scientific value.

Reports to

Head of Medical Affairs

THE OPPORTUNITY

Inventiva is a clinical-stage biopharmaceutical company headquartered in France, focused on the development of lanifibranor in a Phase 3 trial, NATIV3, in MASH. To learn more, please visit: https://inventivapharma.com/

KEY RESPONSIBILITIES

  • Lead the U.S. medical affairs strategy for lanifibranor, aligned with clinical, regulatory, and commercial objectives.
  • Drive medical planning and execution for topline and full data readouts, including scientific interpretation and data dissemination.
  • Provide medical leadership for congress strategy, publications, abstracts, and scientific presentations.
  • Develop core scientific narratives, medical decks, FAQs, and reactive materials in a compliant manner.
  • Build and maintain strong relationships with key opinion leaders (KOLs), investigators, and external experts.
  • Plan and lead advisory boards and scientific exchange activities.
  • Partner cross-functionally with Clinical Development, Regulatory, Commercial, Market Access, and Communications.
  • Support launch readiness, including disease education, unmet need articulation, and evidence-generation planning.
  • Ensure all medical affairs activities are compliant with FDA regulations, PhRMA Code, OIG guidance, and internal policies.

QUALIFICATIONS

  • Advanced scientific or medical degree required (MD, DO, PharmD, PhD, or equivalent)
  • 10+ years of experience in Medical Affairs within biotech or pharmaceutical organizations
  • Proven experience supporting Phase 3 clinical programs and/or major clinical data readouts
  • Pre-launch and/or launch experience strongly preferred
  • Demonstrated success in KOL engagement, advisory boards, and scientific exchange
  • Prior people leadership or matrix leadership experience preferred
  • Strong understanding of U.S. regulatory and compliance requirements for Medical Affairs.

Travel

Approximately 30–40%, including scientific meetings, advisory boards, and internal meetings.

WHY JOIN US

Join Inventiva at a pivotal moment as we prepare for the next phase of growth. This role offers the opportunity to shape the future of Medical Affairs, build a world-class team, and contribute to bringing a potentially transformative therapy to patients with significant unmet medical needs.

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