MAIN PURPOSE OF THE ROLE

Experienced qualified individual contributor that works under limited supervision.

MAIN RESPONSIBILITIES:
- As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills 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.

QUALIFICATIONS

Associates Degree (± 13 years)

Minimum 1 year experience

📌 Medical Advisor (Mumbai)
🏢 Abbott Laboratories
📍 Mumbai