[Hiring] Director, Global Medical Information @Revolution Medicines

Role Description

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.

• Provide therapeutic-area leadership across the Medical Information lifecycle, including strategy, scientific content, launch readiness, contact-center operations support, and customer inquiry management.
• Lead Medical Information related scientific and operational priorities.
• Translate customer insights into actionable recommendations.
• Partner with cross-functional and regional stakeholders to ensure aligned, high-quality Medical Information support.
• Support Medical Information activities at scientific congresses.
• Report to the Head of Medical Information within Global Medical Excellence.

• Develop 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.
• Own 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.
• Collaborate with Clinical Operations, Clinical Development, Biology, Medical Strategy and other internal stakeholders to interpret emerging evidence, identify information needs, and inform content priorities.
• Ensure all medical information content is evidence-based, consistent, and aligned with the latest scientific and clinical data.
• Coordinate with regional leads to support localization, regional review, and country implementation of global medical information resources.
• Support the management of unsolicited inquiries from healthcare professionals, patients, caregivers, ensuring responses are accurate, compliant and timely.
• Serve 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.
• Partner 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.
• Monitor and analyze inquiry trends to identify opportunities for operational improvements and inform the medical strategy.
• Monitor relevant scientific publications, clinical trial results, and treatment developments to inform Medical Information strategy, content updates and training.
• Provide Medical Information support for congresses, including developing resources, staffing Medical Information booths and responding to HCP inquiries.
• Contribute to the development and maintenance of internal SOPs and processes to ensure compliance with regulatory requirements and industry standards.
• Provide support for other Medical Affairs projects as needed.

Qualifications

• 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 decision-making.
• Knowledge of regulatory guidelines related to medical information and safety reporting.
• Proficiency in medical information databases, content management systems and other relevant software tools.
• Experience with Veeva PromoMats advantageous.
• Ability to effectively negotiate and collaborate with internal stakeholders and external partners.
• Ability to prioritize and manage multiple projects simultaneously in a fast-paced dynamic environment.
• Self-motivated with ability to make sound decisions and adapt to changing priorities.
• Experience in managing medical information vendors.
• Willingness to travel, approximately 10-20%.

Preferred Skills

• Minimum of 8 years of experience in Medical Affairs or a related field within the biotech or pharmaceutical industry.
• Experience in the lung cancer therapeutic area strongly preferred.

Benefits

• Competitive cash compensation.
• Robust equity awards.
• Strong benefits.
• Significant learning and development opportunities.

Base Pay Salary Range

$201,000 — $251,000 USD