MAIN RESPONSIBILITIES

- As the Specialist in the Medical Affairs Sub-Function, considered as highly experienced and knowledgeable resource within the organization 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

Education

Education Level

Major/Field of Study or

Equivalent

Associates Degree (± 13 years)

Experience/Background

Experience

Experience Details

Minimum 7 years

Licenses and Certifications

Language Proficiency

Language

Proficiency

📌 Senior Medical Advisor (Mumbai)
🏢 Abbott
📍 Mumbai