Description
You will lead global medical activities for one or more oncology assets and work closely with research, commercial, clinical operations, and local medical teams.
Responsibilities:
- Lead development and delivery of the global medical affairs plan and the integrated evidence plan for oncology assets.
- Drive above-country medical activities such as advisory boards, congress strategy, symposia, and 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.
- Support brand and launch planning by providing medical input to local operating companies and commercial teams.
- Provide medical governance and review scientific materials to ensure accuracy, compliance and clear communication.
Requirements:
- MD, PharmD, or PhD with relevant clinical or scientific experience in oncology.
- 5+ years' experience in medical affairs, clinical development, or related roles in Oncology.
- 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 and proven ability to present complex data clearly.
Preferred Qualifications:
- Deep disease knowledge in 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 and developing early-career medical colleagues.