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Revolution Medicines

Clinical-stage oncology company developing RAS inhibitors

Director – Global Medical Content and Training

Biology & BiotechConfirmed live in the last 24 hours
Full-timeRemote in USA

About the Job

Requirements

  • An advanced scientific or medical degree, specifically a PhD, PharmD, or MD.
  • At least 10 years of experience in Medical Affairs, Scientific Training, or Medical Communications within the biotechnology or pharmaceutical industry.
  • Strong expertise in scientific content development, including booth materials, and training program design for Medical Affairs teams.
  • Demonstrated ability to translate complex scientific data into clear, engaging, and compliant medical content for various stakeholders.
  • Experience developing scientific training curricula, onboarding programs, and continuous learning initiatives.
  • Ability to work cross-functionally with Field Medical, Medical Information, Medical Communications, and Commercial teams to develop consistent messaging and training programs.
  • Deep understanding of industry guidelines, including the PhRMA Code, OIG, ACCME, FDA, and other global regulatory requirements for scientific content and training.
  • Ability to manage multiple priorities in a fast-paced, evolving biotechnology environment.
  • Strong communication, presentation, and interpersonal skills to engage with diverse internal and external audiences.

Responsibilities

  • Oversee development of global congress booth materials, including clinical trial cards, disease state infographics, MOA videos, and related resources.
  • Lead development and execution of selected global Medical Affairs content and training plans.
  • Provide strategic and scientific oversight of the Medical Affairs tactical training roadmap within the learning management system to ensure scientific fluency across the organization.
  • Partner with Regional Medical teams to optimize regionalization of global scientific materials for external engagements, including MSL slide decks, infographics, multimedia, and other scientific-exchange resources.
  • Provide input on decisions and implementation strategy, and manage actions that affect the team's budget.
  • Support implementation of scientific training programs for new hires and ongoing scientific training for MSLs and other Medical Affairs functions.
  • Prepare training curricula to enhance therapeutic area expertise, scientific knowledge, external engagement skills, and competitive insights.
  • Organize scientific deep dives, medical education forums, and training workshops to maintain scientific competency within Medical Affairs.
  • Ensure training programs accommodate different levels of scientific expertise and align with product lifecycle milestones.
  • Implement training assessments to measure learning effectiveness and identify areas for continuous improvement.
  • Lead creation of selected scientific materials for external engagements, including MSL decks, infographics, videos, and training guides.
  • Collaborate with Medical Strategy, Medical Communications, Clinical Development, Regulatory, Commercial, Legal, and Compliance stakeholders to align medical content with company strategy and regulatory and legal requirements.
  • Partner with Medical Affairs leadership to develop a structured pre-launch training plan that prepares the team to support product launch.
  • Work with Field Medical/MSL teams to align scientific training, medical content, and external engagement strategy.
  • Work with Medical Excellence, Field Medical, Medical Communications, Medical Information, and Medical Strategy teams to align training priorities and content needs.
  • Support cross-functional meetings to assess training needs and ensure scientific alignment across the organization.
  • Collaborate with vendor partners to manage development and execution of deliverables.

Desired Qualifications

  • Strong oncology experience, particularly in precision medicine, targeted therapies, or RAS/oncogene-driven cancers.
  • Prior oncology launch experience in Medical Affairs training and scientific content development.
  • Familiarity with digital training platforms, virtual learning solutions, and e-learning modules.
  • Experience with MSL engagement strategies, medical education planning, and congress preparation.
  • Understanding of emerging trends in scientific communication, digital learning, and knowledge management.

About the Company

Revolution Medicines

Clinical-stage oncology company developing RAS inhibitors

Revolution Medicines develops precision oncology drugs focused on cancers driven by RAS mutations. Its RAS(ON) inhibitors are small molecules that bind the active form of RAS to block cancer signaling, with candidates like Daraxonrasib (RMC-6236), Elironrasib (RMC-6291), and Zoldonrasib (RMC-9805) advancing in global Phase 3 trials. The company funds its research through collaborations, royalties, and upfront funding, and has not yet marketed a product. Its goal is to bring effective RAS-targeted therapies to patients and advance multiple candidates through late-stage trials toward approval, supported by strong cash reserves.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Redwood City, CA
Founded
2014

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