MAIN PURPOSE OF THE ROLE Manages teams within the Medical Affairs Sub-Function. Focus is on policy and strategy implementation and control rather than development. Typically handles short-term operational/tactical responsibilities. MAIN RESPONSIBILITIES - As the Manager of the Medical Affairs Sub-Function, oversees the strategy implementation and operations for overseeing the direction, planning, execution, clinical trials/research and the data collection activities. - Contributes to implementation of clinical protocols, and facilitates completion of final reports. - Recruits clinical investigators and negotiates study design and costs. - Responsible for directing human clinical trials, phases III & IV for company products under development. - Participates in adverse event reporting and safety responsibilities monitoring. - Coordinates and provides reporting information for reports submitted to the regulatory agencies.



- Monitors adherence to protocols and determines study completion. - Coordinates and oversees investigator initiations and group studies. - May participate in adverse event reporting and safety responsibilities monitoring. - May act as consultant/liaison with other corporations when working under licensing agreements. QUALIFICATIONS Education Education Level Major/Field of Study or Equivalent Associates Degree (± 13 years) Experience/Background Experience Experience Details Minimum 7 years An Equal Chance Employer Abbot welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities. To request accommodation, please call (phone hidden) or email [email protected]

📌 Regional Medical Affairs Head (Mumbai)
🏢 Abbott
📍 Mumbai