MAIN PURPOSE OF THE ROLELeads/supervises a team of more than 2 professionals within the Medical Affairs Sub-Function.First level manager of a work team that may comprise professionals, technical and/or administrative staff.Typically without budget or hire/fire authority.Focuses on mentoring, coaching, and coordination.MAIN RESPONSIBILITIES
- As the Supervisor of the Medical Affairs Sub-Function, supervises professionals in 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.QUALIFICATIONSEducation Level Major/Field of Study or EquivalentAssociates Degree (± 13 years)Experience/BackgroundMinimum 4 years

📌 Senior Manager Medical Affairs (Maharashtra)
🏢 Abbott
📍 Maharashtra