Revolution Medicines

Senior Director, Global Medical Affairs - GI Oncology

Revolution Medicines$244K — $305K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • Advanced doctorate degree (PharmD, PhD, MD, DO or equivalent) required.
  • 15+ years of experience in Medical Affairs within biotech/pharma, particularly in oncology.
  • Strong background in oncology with emphasis on GI cancers.
  • Hands-on experience in medical affairs functions like medical communications and evidence generation.
  • Proven track record in clinical trial support, including protocol development and site enrollment assistance.
  • Excellent communication skills to convey complex scientific data to varied audiences.
  • Ability to manage multiple priorities in a dynamic environment.

Responsibilities

  • Develop and execute Global Medical Affairs strategy and objectives.
  • Create a Health Care Professional engagement strategy for insights gathering.
  • Serve as the medical representative on cross-functional teams.
  • Act as a content expert in the therapeutic area focused on GI cancers.
  • Participate in the Global Medical Affairs Team to support pre-launch activities.
  • Lead scientific engagement with external stakeholders through advisory boards and congress activities.
  • Collaborate across functions to develop key scientific communication points.

Benefits

  • Competitive cash compensation and robust equity awards.
  • Significant learning and development opportunities.
  • Hybrid work flexibility with travel required.
  • Health care, retirement, and wellness benefits.
Full Job Description

The Opportunity:

Reporting to the GI Tumors Medical Affairs Strategy Lead, the Senior Director, Global Medical Affairs, will be responsible for developing and executing the Global Medical Affairs (GMA) strategy and tactical plans with a focus on launch readiness, launch implementation and life cycle management for an individual asset.

The successful candidate will have a proven track record of developing and driving medical strategies with a focus on effectively communicating key scientific data through publications, medical information, medical communications, and congress activities. The successful candidate will also have experience gathering and analyzing insights through Advisory Boards, Key Opinion Leader (KOL) engagements and interaction with local/regional medical teams and translating those insights into tactics that optimize asset utilization and impact the drug lifecycle.

This role requires close collaboration with cross-functional counterparts across Development, Research and Commercial as well as other internal partners, to design and implement a comprehensive medical affairs strategy for assets in the GI space, with focus on PDAC and CRC.

Key responsibilities:
  • Develops and executes the GMA strategy and medical objectives including activities related to scientific engagement and communication, evidence generation, internal education, and patient advocacy.
  • Develops and executes a Health Care Professional (HCP) engagement strategy to gather insights to shape internal programs.
  • Acts as the medical representative on cross-functional teams.
  • Serves as a therapeutic area content expert.
  • Participates in the Global Medical Affairs Team (GMAT) to execute medical strategies, contribute to the operations and oversight of medical activities, and work cross-functionally to support associated pre-launch activities.
  • Supports the execution of routine gap assessments leading to the development/refinement of publication strategy, evidence generation plans, and tactical plan as part of the overall GMA plan.
  • Provides medical leadership in scientific engagement activities with key external stakeholders through organizing and leading advisory boards, studies investigator interactions, congress activities, and peer-to-peer discussions with the goal of communicating scientific insights to internal teams to drive strategy.
  • Communicates clinical and scientific data to KOLs and other healthcare professionals through presentations, educational programs, and scientific discussions.
  • Represents various medical affairs functions in cross-functional strategy team meetings including Clinical and Safety sub-teams, Global Brand Team, Global Product Team, Patient Advocacy, Market Access, and other cross-functional strategic discussions.
  • Works closely with the Clinical and MSL teams to provide enrollment, scientific, and engagement support to ensure clinical trials meet study timelines.
  • Partners with RWE strategy and Biomarker/CDx teams on related integrated evidence generation strategies and activities as part of the GMA Plan.
  • Works with the Patient Advocacy and Grants teams to incorporate the patient voice and define external medical education strategies for independent grants, respectively.
  • Provides medical support for scientific symposia and medical congresses and collaborate across GMA functions to develop, review, and align on key scientific communication points and medical information response documents within legal and compliance guidelines.
  • Supports the review and approval of abstracts, manuscripts, corporate communications, and other data disclosure documents as well as internal stakeholder medical education activities related to the compound data and related competitor data.
  • Collaborates with stakeholders across the organization, including, but not limited to, Clinical Development and Operations, Commercial Operations, Program Management, Business Development, Regulatory, Safety, and Compliance teams.

Required Skills, Experience and Education:
  • An advanced doctorate degree (PharmD, PhD, MD, DO or equivalent) in medical or scientific area is required.
  • 15+ years of relevant experience in Medical Affairs within the biotech and/or pharmaceutical industry ( local, regional, and global levels) and/or prior clinical oncology practice.
  • Strong scientific background in oncology, with preferred experience in GI cancers, and ability to effectively analyze, synthesize, and communicate complex scientific information.
  • Direct, hands-on experience executing activities across key medical affairs functions, including training, medical communications, medical information, expanded access programs, evidence generation tactics and publications.
  • Proven track record of clinical trial support including protocol development and review, site selection and enrollment support, and data analysis.
  • Excellent interpersonal, written, and presentation skills with the ability to effectively communicate complex scientific data with a strong point of view to diverse audiences.
  • Ability to thrive in a fast-paced, dynamic environment, managing multiple priorities independently with limited supervision.
  • Ability to travel to Redwood City headquarters and professional conferences (30 - 40%).
  • Strong networking skills with deep, existing relationships with GI cancer healthcare professionals, including global key opinion leaders.

Preferred Skills:
  • Experience in global product launches including support of integrated brand plan ideation, regulatory submissions, reimbursement, and label development.
  • Experience in guideline submissions (e.g. NCCN) and engagements with global health authorities preferred.
    #LI-Hybrid #LI-YG1


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.

Base Pay Salary Range

$244,000-$305,000 USD

We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.

Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.

If you believe you've been contacted by someone impersonating a Revolution Medicines recruiter, please report it to [email protected] so we can share these impersonations with our IT team for tracking and awareness.

About Revolution Medicines

Revolution Medicines is a clinical-stage precision oncology company focused on developing targeted therapies to inhibit elusive frontier targets within notorious growth and survival pathways, with particular emphasis on RAS and mTOR signaling pathways. The company's proprietary platform enables the discovery and development of small molecules that bind covalently to proteins. Revolution Medicines was founded in 2014 and is headquartered in South San Francisco, California.
Learn more about Revolution Medicines
Size
201 employees
Market Cap
$2.1 billion
Industry
Net Income
-$108.1 million
Revenue
$42.9 million
NASDAQ

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