Associate Director, Medical Information, Europe

Revolution Medicines is expanding its European Medical Information footprint with a senior leader who can build and guide information access across France and the broader region. The company is a global oncology-focused biopharma working on RAS-addicted cancers, aiming to bring forward innovative medicines through its RAS(ON) tri-complex inhibitors. They combine scientific rigor with a sense of urgency to improve patient outcomes, and this role plays a central part in making trusted medical information available to doctors, patients and caregivers. The Associate Director, Medical Information, Europe will be based onsite in Paris and report to the Director of Medical Information, Europe.

In this position, you’ll help ready Europe for launches, while also supporting ongoing Medical Information needs for both clinical-stage and commercial products. You’ll craft and localize medical information content, support the European call center, and represent MI at scientific congresses. It’s a good fit for a communications-minded science professional who knows France well and can collaborate across local, regional and global teams to keep information accurate and compliant.

If you enjoy translating complex science into clear, compliant guidance, coordinating with cross-functional partners, and shaping how a growing European portfolio communicates with healthcare professionals, this could be a strong match for you.

Guiding information across Europe

Day to day, you’ll lead the creation and maintenance of essential Medical Information resources such as standard response documents, custom response letters, FAQs and guidance for inquiries, ensuring that responses across France and the wider European region are timely and precise. You’ll act as a subject-matter expert for France and the region, balancing regulatory and industry codes with medical accuracy to support MI activities across Europe. The role requires keeping MI content aligned with the latest data, staying compliant with regulatory standards, and responding to unsolicited inquiries from clinicians, patients and caregivers with appropriate speed and quality.

You’ll also monitor inquiry trends and customer insights to identify emerging information needs, inform content development, and suggest operational improvements. In addition, you’ll provide medical information and scientific support related to companion diagnostics tied to therapeutic assets, ensuring consistent messaging across stakeholders. Expect to staff European congresses or national events as needed, prepare congress-specific MI resources, and partner with a MI vendor and call center team to maintain training and delivery of accurate, compliant responses, including France-specific requirements. You’ll contribute to the ongoing development and maintenance of SOPs, work instructions and processes to stay compliant, and you’ll help track activity and outcomes to brief leadership and cross-functional partners. Finally, you’ll keep a watchful eye on scientific publications and trial data to keep content current and credible.

What you’ll need to bring to the team

What matters most are the essentials that confirm you can lead in this European context and deliver trustworthy information across multiple markets.

• An advanced degree in a scientific or medical field, with a PhD, MD or PharmD preferred
• Eight or more years in Medical Affairs, including at least five years in Medical Information
• Proven track record supporting MI activities in France and operating within European and global MI structures
• Solid understanding of EU Medical Information principles and compliance requirements
• Experience coordinating MI activities across local and regional settings
• Background in oncology and familiarity with launch readiness programs
• Demonstrated medical information experience in the pharmaceutical or biotechnology industry
• Excellent verbal and written communication in both French and English
• Ability to create, review and manage scientific content for diverse audiences
• Strong organizational, problem-solving and project-management skills
• Collaborative mindset with the ability to work with cross-functional teams across local, regional and global levels
• Self-motivated with sound judgment, autonomy and adaptability to changing priorities
• Proficiency with medical information databases, content management systems and related tools
• Experience with Veeva PromoMats is advantageous
• Experience overseeing medical information vendors
• Willingness to travel about 10–20%

• Nice to have: experience shaping communications around companion diagnostics tied to therapies
• Nice to have: hands-on vendor-management experience in a Medical Information context
• Nice to have: exposure to European congresses and national events across multiple markets

Compensation and logistics

The role is onsite in Paris, with the description noting possible base locations in Switzerland or France and a reporting line to the Director of Medical Information, Europe. You should expect travel to be in the ballpark of 10–20%. Specific salary and benefits are not disclosed in the materials provided.

Advice for applicants

Put your strongest qualification up front. In your resume, lead with your advanced degree and your MI leadership experience, then show concrete evidence of eight-plus years in Medical Affairs and at least five in Medical Information, with clear France and wider European exposure.

Show how you prove the must-have skills. Tie your experience to creating and managing MI content such as SRDs, CRLs and FAQs, plus how you’ve kept materials compliant with EU rules and adaptable for local markets. Include examples of cross-functional projects where you collaborated with regional or global teams, and highlight your French-English communication prowess.

Prepare for interviews by recounting scenarios where you handled multiple priorities and balanced regulatory requirements with scientific accuracy. Be ready to discuss your approach to responding to unsolicited inquiries from clinicians or patients, and how you’ve supported MI around congresses or launch activities in Europe.

Think of a thoughtful question to ask. A good one would explore how the European MI function plans for upcoming product launches across multiple markets and how this role interacts with the MI vendor, call center operations and congress activities to ensure consistent, compliant messaging.