Senior Director, Global Medical Affairs - GI Oncology

About the role

The Senior Director, Global Medical Affairs will develop and execute the Global Medical Affairs strategy and tactical plans with a focus on launch readiness, launch implementation, and life cycle management for an individual asset. They will lead the development of medical strategies, gather insights through Advisory Boards and KOL engagements, and translate those insights into tactics that optimize asset utilization and impact the drug lifecycle.

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 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 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.
• PARTNER 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 COLLABORATES 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.

Requirements

• 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.

Qualifications

• Required:
• Advanced doctorate degree (PharmD, PhD, MD, DO or equivalent)
• 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
• Direct, hands-on experience executing activities across key medical affairs functions
• Proven track record of clinical trial support
• Excellent interpersonal, written, and presentation skills
• 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

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

Benefits

Base Pay Salary Range: $244,000 - $305,000 USD

Pay

Base Pay Salary Range: $244,000 - $305,000 USD

Schedule

Full-time

Company

Revolution Medicines

Contact

For additional information, please contact privacy@revmed.com.