Ex
Posted:
June 01, 2026
Location:
ottawa, on, Canada
Job Description
Key Responsibilities
- Critical evaluation of clinical data of the investigational products/similar drugs from clinical sciences perspective to build a foundation for clinical development strategies for registration purposes or for evaluation of in-licensing opportunities.
- Closely collaborates with various teams (including Clinical Development team members, Project Management, Clinical Operations, Pharmacovigilance, Regulatory, Global Medical Affairs, Intellectual Property) for clinical development planning, protocol development & finalization, execution support, regulatory presentations and HA interactions etc.
- Medical monitoring and supervision of the clinical oncology studies.
- Develops and maintains collaborative partnerships with oncology stakeholders, key external experts, and allied health professionals ensuring scientific understanding and advocacy around products and therapeutic area.
- Closely collaborates with portfolio, bus...
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Job Type:
Full-time
Location:
ottawa, Canada
Posted:
June 01, 2026
Deadline:
July 11, 2026