Associate Director, Global Medical Information

Revolution Medicines, Inc.; United States; Remote; USD 177,000 - 221,000; Full time

Job summary

Revolution Medicines is seeking an Associate Director of Medical Information to lead the development, review and maintenance of Medical Information content. You will respond to inquiries, support congress activities, and collaborate with Medical Affairs, Regulatory, and Commercial teams to ensure compliant, evidence-based information across the product lifecycle.

The role requires an advanced degree and experience in pharma/biotech Medical Information, with 10–20% travel.

Qualifications

• Advanced degree in scientific or medical discipline; doctoral degree preferred.
• Experience supporting Medical Information in pharma/biotech.
• Excellent verbal and written communication skills.
• Experience creating and managing scientific content for diverse audiences.
• Strong organizational, problem solving and project management skills.
• Collaborates effectively with cross-functional stakeholders.
• Self-motivated with autonomy and adaptability to changing priorities.
• Proficiency with medical information databases and CMS.

Responsibilities

• Develops, reviews and maintains Medical Information resources (SRDs, CRLs, FAQs).
• Ensures content is scientifically accurate, evidence-based and compliant.
• Supports unsolicited inquiries from HCPs, patients and caregivers.
• Monitors inquiry trends to inform content development and operations.
• Provides Medical Information for companion diagnostics communications.
• Supports Medical Information at scientific congresses and staffing booths.
• Develops and maintains SOPs and operational processes for compliance.
• Monitors publications and trial data to inform content strategy.
• Collaborates with Medical Affairs, Clinical Development, Regulatory, Safety and others to support launch readiness.
• Provides Medical Information expertise for additional Medical Affairs initiatives.

Skills

Communication skills

Project management

Cross-functional collaboration

Scientific content creation

Medical information

Verbal communication

Autonomy

Veeva PromoMats

Education

PharmD/MD/PhD preferred

Advanced degree in science/medicine

Tools

Veeva PromoMats

Content Management Systems

Medical information databases

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 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 strong scientific background, demonstrated Medical Information expertise, and ability to manage multiple priorities in a dynamic environment.

Key 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.
• Partner 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.

Required Skills, Experience and Education:

• 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 audience.
• 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.
• Experience with Veeva PromoMats preferred.
• 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 oncology therapeutic area; experience supporting launch readiness preferred.

#LI-VN1 #LI-Remote

The base pay salary range for this full‑time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job‑related skills, experience, market dynamics, and relevant education or training.

Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.

Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact [e-mail].

Base Pay Salary Range

$177,000—$221,000 USD