Regional Medical Advisor

Abbott Laboratories; Lucknow; On-site; INR 800,000 - 1,500,000; Full time

Job summary

Abbott Laboratories in Lucknow, India seeks an Experienced Medical Affairs professional to contribute under limited supervision. The role applies subject matter knowledge to clinical trials planning, execution and data collection, with responsibilities spanning protocol implementation and safety monitoring.

The position involves coordinating investigator-related activities, study design discussions, and regulatory reporting, ensuring protocol adherence and successful study completion in

Qualifications

• Associates Degree (± 13 years).
• Experience: Minimum 1 year in relevant field.

Responsibilities

• Oversee direction, planning and execution of clinical trials.
• Coordinate data collection and reporting for studies.
• Participate in adverse event reporting and safety monitoring.
• Engage with investigators, study design and costs negotiation.
• Ensure compliance with protocols and regulatory submissions.
• Liaise with other organizations under licensing agreements.

Skills

Clinical trials

Data collection

Regulatory reporting

Education

Associates Degree

Job description

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