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...