Revolution Medicines - Redwood City, CA

posted 15 days ago

Full-time - Senior
Redwood City, CA
Professional, Scientific, and Technical Services

About the position

The Senior Director, Global Medical Strategy for Pancreatic Ductal Adenocarcinoma (PDAC) at Revolution Medicines is a pivotal role within the Medical Affairs team. This position is responsible for developing and executing the Global Medical Affairs strategy and tactical plans focused on launch readiness and life cycle management for PDAC therapies. The successful candidate will collaborate with cross-functional teams to drive medical strategy, communicate scientific data, and engage with key opinion leaders and stakeholders in the oncology field.

Responsibilities

  • Develop and execute the multi-year global and US medical strategy for PDAC.
  • Oversee the publication and medical communications strategy, integrated evidence planning, lifecycle management, and budget planning process.
  • Support the GI Global Medical Affairs Team to execute medical strategies and contribute to the operations and oversight of medical activities associated with PDAC.
  • Provide regular updates and support to senior leadership regarding medical strategy and activities.
  • Lead integrated evidence generation planning in PDAC, including conducting routine cross-functional gap assessments.
  • Organize and lead PDAC advisory boards, study investigator interactions, and congress activities to communicate scientific insights.
  • Support medical contribution to cross-functional strategy team meetings including Clinical and Safety sub-teams and product teams.
  • Work closely with Clinical and MSL teams to provide enrollment, scientific, and engagement support for clinical trials.
  • Partner with RWE strategy and translational teams on integrated evidence generation strategies.
  • Incorporate the patient voice and define external medical education strategies in collaboration with Patient Advocacy.
  • Support competitive intelligence team activities through landscape assessments and development of patient journey insights.
  • Provide medical support for scientific symposia and medical congresses, ensuring alignment on key scientific communication points.
  • Review and approve abstracts, manuscripts, and corporate communications related to compound data and competitor data.
  • Provide medical strategy leadership for expanded access programs and investigator sponsored research for PDAC.
  • Manage budgets and resources efficiently for GMA supported activities in PDAC.

Requirements

  • An advanced doctorate degree (PharmD, PhD, MD, DO or equivalent) in a medical/scientific area is required.
  • Minimum of ten years of experience in academic medicine, biotech, and/or pharmaceutical industry, with at least five years in oncology research and/or patient care.
  • Strong scientific background in oncology with a good understanding of biomarker-driven disease.
  • Ability to analyze, synthesize, and communicate complex scientific information effectively.
  • Strong networking skills with existing relationships with oncology healthcare professionals, including global top key opinion leaders.
  • Experience in KOL mapping and development of engagement plans.
  • Previous responsibility for medical affairs activities, including budget management for multiple compounds.
  • Direct experience executing activities within medical affairs such as training, medical communications, and evidence generation.
  • Extensive experience in global product launches and support of integrated brand plan ideation.
  • Proven track record of clinical trial support including protocol development and site selection support.
  • Experience conducting gap assessments and executing evidence generation plans.

Nice-to-haves

  • Experience in guideline submissions (e.g. NCCN) and engagements with global health authorities.

Benefits

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