Senior Director, Global Medical Director – GI Tumors

This is a fully remote position, open to applicants in United States, +3 more locations.

📋 Description

• Lead the GI Cancer Global Medical functional matrix team.

• Collaborate with US and EUR/INT Medical Affairs teams to comprehend regional customer, patient, healthcare provider, and healthcare system needs and priorities.

• Represent and advocate for medical perspectives within global cross-functional teams and governance forums, including CDT, LDT, PGC, and DPRC.

• Contribute Medical Affairs expertise to early development activities, such as TPP development, clinical trial design, and lifecycle planning.

• Ensure that regional needs and insights are integrated into clinical development discussions, evidence-generation activities, and lifecycle planning.

• Maintain and utilize knowledge of the competitive landscape to guide evidence-generation strategy and internal development decisions.

• Direct the development, maintenance, and execution of the Integrated Evidence Generation Plan for solid tumor oncology products in BTC, gastroesophageal cancer, and other GI malignancies.

• Collaborate with Medical Affairs, Clinical Development, Regulatory Affairs, Market Access, HEOR, RWE, Commercial, and other cross-functional teams.

• Oversee and support evidence-generation activities, including investigator-sponsored studies, real-world evidence initiatives, health outcomes research, and Phase IV interventional studies.

• Lead the creation of the breast cancer medical narrative by identifying and advancing analytic needs and guiding the interpretation of pivotal trial data.

• Provide leadership and input from Medical Affairs into the Payor Value and Evidence Plan.

• Direct the development and implementation of publication strategy and evidence dissemination plan.

• Assist with scientific communications, congress planning, advisory boards, and external engagement activities.

• Serve as a subject matter expert for internal cross-functional stakeholders.

⛳️ Requirements

• A minimum of 10 years of experience in Medical Affairs, Clinical Development, or a related field within the pharmaceutical or biotechnology industry.

• Oncology experience is preferred.

• Strongly preferred experience in GI cancers and/or HER2-targeted therapies.

• Proven experience in developing and executing evidence-generation strategies, publication plans, and external scientific engagement activities.

• Comprehensive understanding of clinical research, evidence generation, and oncology drug development.

• Ability to influence without authority and effectively operate within complex matrix organizations.

• Strong strategic thinking and operational execution capabilities.

• Excellent written, verbal, presentation, and stakeholder management skills.

• Capability to build productive partnerships across regions and functions.

• Ability to manage multiple priorities and deliver high-quality outcomes in a fast-paced environment.

• Desired experience in lifecycle management of oncology indications.

• An advanced scientific or healthcare degree is required (PharmD, PhD, MD, MBBS, Nurse Practitioner, PA, or equivalent).

• Preferred experience in the delivery of oncology care.

🏝️ Benefits

• Discretionary annual cash bonus or incentive compensation.

• Discretionary equity grants through the Long Term Equity Incentive Plan.

• Medical insurance.

• Dental insurance.

• Vision insurance.

• 401k retirement savings plan.

• Flexible paid vacation.