Regional Medical Advisor

Abbott; Lucknow; On-site; INR 700,000 - 1,100,000; Full time

Job summary

Abbott India is seeking an experienced Medical Affairs professional to act as an individual contributor under limited supervision. The role focuses on applying subject matter knowledge to clinical trials, data collection, and regulatory reporting for our products.

You will oversee protocol implementation, recruit investigators, coordinate reporting, and support safety monitoring across phases III and IV, collaborating with cross-functional teams and external partners.

Qualifications

• Associates degree required; relevance to medical affairs preferred.
• Minimum 1 year of experience in medical affairs or a related field.

Responsibilities

• Oversee direction, planning, and execution of clinical trials and data collection activities.
• Contribute to implementation of clinical protocols and final reports.
• Recruit clinical investigators and negotiate study design and costs.
• Direct human clinical trials, phases III and IV for products under development.
• Participate in adverse event reporting and safety monitoring.
• Coordinate reporting for regulatory submissions and agency reports.
• Monitor adherence to protocols and study completion.
• Coordinate investigator initiations and group studies.
• May liaise with other corporations under licensing agreements.
• May participate in adverse event reporting and safety responsibilities monitoring.

Skills

Associates Degree

Education

Associates Degree

Job description

MAIN PURPOSE OF ROLE

Experienced professional individual contributor that works under limited supervision.

MAIN PURPOSE OF ROLE

Experienced professional individual contributor that works under limited supervision.

Applies subject matter knowledge in the area of Medical Affairs.

Requires capacity to apply skills/knowledge within the context of specific needs or requirements.

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

Education

Education Level : Associates Degree (± 13 years)

Experience/Background

Experience : Minimum 1 year