**_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_

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]

Required Skill Profession

Other General

📌 Senior Medical Advisor (Mumbai)
🏢 Abbott
📍 Mumbai