[Hiring] Senior Director, Medical Information @Revolution Medicines

Role Description

We are seeking a motivated and experienced professional to join our team as Senior Director of Medical Information supporting the European region. 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, you will:

• Oversee the creation and management of medical information content.
• Provide scientific and operational oversight of the European medical information call center team.
• Contribute to medical booth asset creation.
• Contribute to dossier development and review.
• Provide Medical Information support at scientific congresses.
• Collaborate cross-functionally to support both pipeline assets and companion diagnostics.

The ideal candidate is a skilled communicator with a strong scientific background and can manage projects in a dynamic environment. This role will be based in Europe, and will report to the Head of Medical Information within the Global Medical Excellence team.

Qualifications

• Advanced degree in scientific or medical discipline; doctoral degree preferred (PharmD, MD, PhD).
• 11+ years relevant experience (PhD), 13+ years (MSc).
• Experience in oncology therapeutic area.
• Proven experience in medical information, preferably 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%.

Requirements

• Develops, reviews and maintains medical information resources such as standard response letters (SRLs), custom response letters (CRLs), FAQs and inquiry response guidance documents to support accurate and timely responses to customers.
• Collaborates with Clinical Operations, Clinical Development, Biology and other internal stakeholders to gather insights for medical information content creation.
• Ensures all medical information content is evidence-based, consistent, and aligned with the latest scientific and clinical data.
• Supports the management of unsolicited inquiries from healthcare professionals, patients, caregivers, ensuring responses are accurate, compliant and timely.
• Serves as Medical Reviewer in the Medical, Legal and Regulatory (MLR) process, ensuring that materials support evidence-based communication and comply with company policies, industry standards, and regulatory requirements.
• Leads or contributes to the development, review and maintenance of dossiers to support market access and payer engagement strategies.
• Collaborates with cross-functional partners to provide strategic medical insights and ensure scientific accuracy in promotional and non-promotional materials.
• Monitors and analyzes inquiry trends to identify opportunities for operational improvements and inform the medical strategy.
• Provides medical information and scientific support related to companion diagnostics associated with therapeutic assets, ensuring aligned communication across stakeholders.
• Supports the compendia submission process for Medical Affairs.
• Provides Medical Information support for congresses, including developing resources, staffing Medical Information booths and responding to HCP inquiries.
• Leads the development and maintenance of internal SOPs and processes to ensure compliance with regulatory requirements and industry standards.
• Trains and support Medical Information call center vendor to deliver accurate, compliant and high-quality responses to inquiries.
• Prepares and presents regular reports on medical information performance metrics and outcomes to senior management.
• Monitors relevant scientific publications and clinical trial data to inform medical information content and strategy.
• Provides support for other Medical Affairs projects as needed.

Company Description

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins.

The company’s RAS(ON) inhibitors currently in clinical development include:

• daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor;
• elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor;
• zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor;
• RMC-5127, a RAS(ON) G12V-selective inhibitor.

As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.