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, business development, Global medical affairs team ...