Director, Field Medical Advisor

Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.

Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.

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 Spain. 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 Spain.

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 German 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.

• Develop and implement an early pre-launch German 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 Spain.
• 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 German 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.

• 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 German 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%).

• Prior experience in oncology product launches.
• Strong network within the German oncology community.
• Experience in investigator-initiated or real-world evidence studies.
• Knowledge of German healthcare systems, reimbursement structures, and compliance requirements.
• Track record in publication planning, congress presentations, and scientific communications.

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