Define and drive the clinical strategy for the assigned care area (oncology)
Lead the development of Target Product Profiles (TPPs), Integrated Evidence Generation Plans (IEGPs), and clinical development plans
Represent the therapeutic area in governance forums and regulatory interactions
Engage with KOLs and external experts to shape development strategy
Oversee cross-functional alignment across Regulatory, Medical Affairs, Commercial, and Clinical Operations
Mentor and guide clinical scientists and medical monitors working within the care area
Provide medical oversight for one or more clinical trials
Review safety data, assess adverse events, and support dose modifications or protocol amendments
Respond to investigator queries and support site engagement
Participate in Data Safety Monitoring Boards (DSMBs) and internal safety reviews
Contribute to clinical study reports (CSRs), regulatory submissions, and medical writing
Collaborate with Clinical Operations and Pharmacovigilance teams

Senior Medical Director

Key skills