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Revolution Medicines

Director, Field Medical Advisor, France

RemoteFrance only
Published
Experience
Lead
Salary not disclosed
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Open to FR only. Set where you work from to check your eligibility.

No BS summary

Director-level field medical affairs role for France, requiring 8–10 years in pharma/biotech Medical Affairs or related functions, advanced medical/scientific degree, and strong oncology clinical development knowledge. Must be fluent in French and English and able to travel nationally and internationally up to 25%.

Required languages

French Fluent / written and spoken stipulated as fluency required specified in posting: Fluency in French and English (written and spoken).; required=true omitted by schema constraints.English Fluent / written and spoken stipulated as fluency required specified in posting: Fluency in French and English (written and spoken).; required=true omitted by schema constraints.

What you'll do

  • Develop and implement an early pre-launch French Medical Affairs strategy and tactical plan for assigned products and therapeutic areas.
  • Establish and maintain trusted scientific relationships with key opinion leaders (KOLs), investigators, and healthcare professionals across France.
  • Provide medical oversight and scientific input to cross-functional teams, ensuring alignment with regulatory and compliance standards.
  • Collaborate with other Medical Science Liaisons, Medical Affairs, and clinical research departments to support scientific exchange, education, and data dissemination activities.
  • Contribute to medical input in promotional and non-promotional materials, internal training, and advisory boards.
  • Plan and execute national medical meetings, symposia, and congress participation to enhance scientific visibility.
  • Support investigator-initiated trials and local clinical research activities in collaboration with global and regional teams.
  • Monitor the competitive and scientific landscape to inform internal strategy and provide actionable medical insights.
  • Partner with HEOR and market access to develop real-world evidence and outcomes research projects.
  • Ensure compliance with French and EU regulatory frameworks governing interactions with healthcare professionals.
  • Collaborate closely with Clinical Operations and CROs, including site selection, Site Initiation Visits, and investigator engagement.

What they require

  • Advanced scientific or medical degree (MD, PharmD, or PhD) required; oncology experience strongly preferred.
  • Minimum 8-10 years of experience in Medical Affairs or related functions in the pharmaceutical or biotech industry.
  • Strong understanding of oncology clinical development, evidence generation, and treatment landscape.
  • Proven ability to interpret and communicate complex scientific and clinical data.
  • Experience engaging with healthcare professionals, academic researchers, and medical societies.
  • Excellent interpersonal, organizational, and presentation skills.
  • Fluency in French and English (written and spoken).
  • Ability to work effectively in a matrixed, cross-functional, and multicultural environment.
  • Willingness to travel nationally and internationally (up to 25%).
  • Preferred: Prior experience in oncology product launches.
  • Preferred: Strong network within the French oncology community.
  • Preferred: Experience in investigator-initiated or real-world evidence studies.
  • Preferred: Knowledge of French healthcare systems, reimbursement structures, and compliance requirements.
  • Preferred: Track record in publication planning, congress presentations, and scientific communications.
🇺🇸 United StatesPharmaceuticalsMid-sizerevmed.com/

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