Associate Director, Global Medical Information

Revolution Medicines

11d•$177,000 - $221,000•Hybrid

About The Position

Revolution Medicines is a global, commercial-stage 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 motivated and experienced professional to join our Global Medical Information team as an Associate Director of Medical Information. This role focuses on ensuring the delivery of timely, accurate, and evidence-based responses to healthcare professionals (HCPs), patients, and caregivers. As a key member of the Medical Affairs team, this individual will support the development and execution of Medical Information activities across the product lifecycle, including the creation and maintenance of scientific response content, support of Medical Information contact center operations, and scientific congresses. The ideal candidate is a skilled communicator with a strong scientific background, demonstrated Medical Information expertise, and the ability to manage multiple priorities in a dynamic environment.

Requirements

Advanced degree in a scientific or medical discipline; doctoral degree preferred (PharmD, MD, PhD).
Experience supporting Medical Information activities within the pharmaceutical or biotechnology industry, including familiarity with applicable regulatory and compliance requirements.
Excellent verbal and written communication skills.
Experience creating, reviewing, and managing scientific content for diverse audiences.
Strong organizational, problem-solving, and project management skills.
Demonstrated ability to collaborate effectively with cross-functional stakeholders and external partners.
Self-motivated, with the ability to exercise sound judgment, work with appropriate autonomy, and adapt to changing priorities.
Proficiency in medical information databases, content management systems, and other relevant software tools.
Willingness to travel, approximately 10-20%.

Nice To Haves

Experience with Veeva PromoMats preferred.
Minimum of 8 years of experience in Medical Affairs or a related field within the biotech or pharmaceutical industry.
Experience in oncology therapeutic area; experience supporting launch readiness preferred.

Responsibilities

Develops, reviews, and maintains Medical Information resources, including standard response documents (SRDs), custom response letters (CRLs), FAQs, and other approved response materials.
Ensures all Medical Information content is scientifically accurate, evidence-based, consistent with the latest clinical data, and compliant with applicable regulatory requirements, industry codes, and medical information standards.
Supports the management of unsolicited inquiries from healthcare professionals, patients, and caregivers, ensuring responses are accurate, compliant, and timely.
Monitors and analyzes Medical Information inquiry trends and customer insights to identify emerging scientific information needs, inform content development, and recommend operational improvements.
Provides Medical Information and scientific support related to companion diagnostics associated with therapeutic assets, ensuring aligned communication across relevant stakeholders.
Supports Medical Information activities at scientific congresses, including preparation of congress-specific Medical Information resources and staffing Medical Information booths.
Contributes to the development, implementation, and maintenance of Medical Information SOPs, work instructions, and operational processes to support compliance with applicable regulatory requirements, industry standards, and company policies.
Monitors relevant scientific publications and clinical trial data to inform Medical Information content and strategy.
Partners cross-functionally with Medical Affairs, Clinical Development, Regulatory, Legal/Compliance, Safety, Commercial, and other stakeholders to support launch readiness and product lifecycle needs.
Provides Medical Information expertise and support for additional Medical Affairs initiatives and projects as needed.