Medical Advisor, France

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers.  The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding Revolutionaries in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

Revolution Medicines is seeking a highly motivated and scientifically driven field based and customer facing Director Medical Liaison / Medical Advisor to jump start Medical Affairs activities in France. This role will report in the beginning to the SVP Head of Europe until a VP Head of Medical Affairs Europe has joined, and later on to the Senior Medical Director France. This position will be instrumental in driving the scientific excellence, clinical insight, and medical strategy supporting our oncology pipeline and marketed products. The field based Director Medical Liaison / Medical Advisor will serve as the medical expert within the upcoming French affiliate, ensuring scientific integrity and alignment with global and European medical affairs and clinical objectives. The position will require close collaboration with cross-functional partners including clinical development, clinical operations, regulatory, commercial, HEOR, market access, and other field medical teams across Europe.

Key Responsibilities

• 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

Required Skills, Experience and Education:

• 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 Skills:

• Prior experience in oncology product launches

• Strong network within the French oncology community.

• Experience in investigator-initiated or real-world evidence studies.

• Knowledge of French healthcare systems, reimbursement structures, and compliance requirements.

• Track record in publication planning, congress presentations, and scientific communications

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