Director, Global Medical Information

revolutionmedicines; United States; On-site; USD 180,000 - 280,000; Full time

Job summary

Revolution Medicines seeks a Director of Medical Information to lead timely, evidence-based medical information for HCPs, patients and caregivers. You will shape strategy, oversee content plans, and coordinate global Medical Information resources across regions, ensuring compliant, data-driven communications.

The ideal candidate has 10+ years in oncology medical information, advanced degree, and proven leadership in cross-functional teams, with strong writing and analytics capabilities to

Qualifications

• Advanced degree in scientific or medical discipline; doctoral degree preferred (PharmD, MD, PhD).
• 10+ years relevant experience in oncology medical information.
• Experience evaluating clinical trial data and communicating complex scientific information.
• Proven experience in medical information within the pharmaceutical/biotech industry.
• Excellent verbal and written communication skills.
• Experience creating, reviewing and managing scientific content for diverse audiences.
• Strong organizational, problem-solving and project management skills.
• Strong analytical skills to monitor and analyze data to inform strategy.

Responsibilities

• Develops and executes Medical Information strategy and therapeutic-area priorities for assigned area.
• Owns the Medical Information content plan, including standard/FAQs, response letters and guidance.
• Collaborates with Clinical Operations, Clinical Development, Biology and Medical Strategy to interpret evidence and inform content priorities.
• Ensures medical information content is evidence-based and aligned with latest data.
• Coordinates with regional leads to support localization, review and country implementation.
• Supports management of unsolicited inquiries ensuring accuracy, compliance and timeliness.
• Acts as medical reviewer for materials through MLR process.
• Partners on agent training, content deployment and inquiry escalation with MICC lead and vendors.
• Monitors inquiry trends to identify operational improvements and inform medical strategy.
• Monitors publications and trial results to inform strategy, content updates and training.
• Provides support for congresses, staffing booths and responding to inquiries.
• Contributes to SOPs to ensure regulatory compliance and industry standards.

Skills

Medical Information

Content strategy

Regulatory compliance

Stakeholder leadership

Scientific writing

Education

Advanced degree

Job description

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.

The Opportunity:

We are seeking a strategic and experienced professional to join our team as Director of Medical Information. This role will lead the delivery of timely, accurate, and evidence-based Medical Information to healthcare professionals (HCPs), patients, and caregivers.

As a key member of the Medical Affairs team, you will provide therapeutic-area leadership across the Medical Information lifecycle, including strategy, scientific content, launch readiness, contact-center operations support, and customer inquiry management. The role will lead Medical Information related scientific and operational priorities; translate customer insights into actionable recommendations; and partner with cross-functional and regional stakeholders to ensure aligned, high-quality Medical Information support. The Director will also support Medical Information activities at scientific congresses. The ideal candidate is a skilled communicator and people leader with strong scientific acumen, demonstrated Medical Information expertise, and the ability to lead complex initiatives in a dynamic environment. The role will report to the Head of Medical Information within Global Medical Excellence.

• Develops and execute Medical Information strategy and therapeutic-area priorities for assigned therapeutic area in alignment with Medical Strategy leads, regional Medical Information teams, and other key stakeholders.
• Owns the Medical Information content plan, including the development, review, approval, deployment, and maintenance of standard response letters, custom response letters, FAQs, inquiry response guidance, and special handling instructions.
• Collaborates with Clinical Operations, Clinical Development, Biology, Medical Strategy and other internal stakeholders to interpret emerging evidence, identify information needs, and inform content priorities.
• Ensures all medical information content is evidence-based, consistent, and aligned with the latest scientific and clinical data.
• Coordinates with regional leads to support localization, regional review, and country implementation of global medical information resources.
• Supports the management of unsolicited inquiries from healthcare professionals, patients, caregivers, ensuring responses are accurate, compliant and timely.
• Serves as medical reviewer for therapeutic-area materials through the Medical, Legal and Regulatory (MLR) process, ensuring that materials support evidence-based communication and comply with company policies, industry standards, and applicable regulatory requirements.
• Partners with the MICC lead and Medical Information vendors on agent training, content deployment, response quality, and inquiry escalation. Contribute to vendor performance reviews and corrective actions within the role's therapeutic-area scope.
• Monitors and analyzes inquiry trends to identify opportunities for operational improvements and inform the medical strategy.
• Monitors relevant scientific publications, clinical trial results, and treatment developments to inform Medical Information strategy, content updates and training.
• Provides Medical Information support for congresses, including developing resources, staffing Medical Information booths and responding to HCP inquiries.
• Contributes to the development and maintenance of internal SOPs and processes to ensure compliance with regulatory requirements and industry standards.
• Provides support for other Medical Affairs projects as needed.

Required Skills, Experience and Education:

• Advanced degree in scientific or medical discipline; doctoral degree preferred (PharmD, MD, PhD).
• 10+ years relevant experience.
• Experience in oncology therapeutic area and demonstrated ability to critically evaluate clinical trial data and communicate complex scientific information.
• Proven experience in medical information within the pharmaceutical or biotechnology industry.
• Excellent verbal and written communication skills.
• Experience creating, reviewing and managing scientific content for diverse audience.
• Strong organizational, problem-solving and project management skills.
• Strong analytical skills with the ability to monitor and analyze data to inform