Global Medical Director, Oncology
GSK
August 07, 2026
Remote friendly (Philadelphia, PA)
United States
Medical Affairs
Responsibilities:
- Lead development and delivery of the global medical affairs plan and integrated evidence plan for oncology assets.
- Drive above-country medical activities (advisory boards, congress strategy, symposia, scientific education).
- Own scientific engagement with external experts, patients, payers, and regulators to gather insights and shape strategy.
- Partner with research and development to design and prioritize global and supportive clinical studies, including review of investigator-initiated proposals.
- Provide medical input to local operating companies and commercial teams to support brand and launch planning.
- Provide medical governance and review scientific materials to ensure accuracy, compliance, and clear communication.
Qualifications (Required):
- MD, PharmD, or PhD with relevant clinical or scientific experience in oncology.
- 5+ years’ experience in medical affairs, clinical development, or related oncology roles.
- Demonstrated experience leading global medical strategies and evidence generation plans.
- Strong understanding of clinical trial design and operational experience with global studies.
- Experience engaging external experts, advisory boards, and congress planning.
- Excellent written and verbal communication in English; ability to present complex data clearly.
Qualifications (Preferred):
- Deep disease knowledge in prostate or lung oncology.
- Experience with expanded access programs or post-approval study requirements.
- Prior experience working across time zones and in a matrix global organization.
- Familiarity with promotional review processes and medical governance standards.
- Track record of publications/abstracts or congress leadership.
- Experience mentoring early-career medical colleagues.
How to Apply:
- Submit your CV and a short cover letter explaining why the role matters to you and how you would contribute.
- Lead development and delivery of the global medical affairs plan and integrated evidence plan for oncology assets.
- Drive above-country medical activities (advisory boards, congress strategy, symposia, scientific education).
- Own scientific engagement with external experts, patients, payers, and regulators to gather insights and shape strategy.
- Partner with research and development to design and prioritize global and supportive clinical studies, including review of investigator-initiated proposals.
- Provide medical input to local operating companies and commercial teams to support brand and launch planning.
- Provide medical governance and review scientific materials to ensure accuracy, compliance, and clear communication.
Qualifications (Required):
- MD, PharmD, or PhD with relevant clinical or scientific experience in oncology.
- 5+ years’ experience in medical affairs, clinical development, or related oncology roles.
- Demonstrated experience leading global medical strategies and evidence generation plans.
- Strong understanding of clinical trial design and operational experience with global studies.
- Experience engaging external experts, advisory boards, and congress planning.
- Excellent written and verbal communication in English; ability to present complex data clearly.
Qualifications (Preferred):
- Deep disease knowledge in prostate or lung oncology.
- Experience with expanded access programs or post-approval study requirements.
- Prior experience working across time zones and in a matrix global organization.
- Familiarity with promotional review processes and medical governance standards.
- Track record of publications/abstracts or congress leadership.
- Experience mentoring early-career medical colleagues.
How to Apply:
- Submit your CV and a short cover letter explaining why the role matters to you and how you would contribute.