Regional Medical Advisor

Abbott Laboratories; Delhi; On-site; INR 1,800,000 - 3,000,000; Full time

Job summary

Abbott Laboratories in New Delhi, India, is seeking experienced medical professionals to lead clinical trial oversight and data collection activities within Medical & Scientific Affairs. The role focuses on planning, execution of trials, safety monitoring, and regulatory reporting in collaboration with investigators and external partners.

The position emphasizes adherence to protocols and the ability to liaise with regulatory bodies, ensuring compliant study conduct across Phases III and IV.

Qualifications

• Experience in medical affairs or clinical research.
• Ability to oversee clinical protocols and data collection.
• Experience liaising with regulatory agencies and licensors.

Responsibilities

• Oversee direction, planning, and execution of clinical trials (Phases III & IV).
• Coordinate and provide reporting information to regulatory agencies.
• Recruit investigators and negotiate study design and costs.
• Monitor adherence to protocols and determine study completion.
• Contribute to adverse event reporting and safety responsibilities.
• May act as consultant/liaison with other corporations under licensing agreements.

Skills

Clinical trial oversight

Adverse event reporting

Regulatory compliance

Job description

JOB DESCRIPTION:

Main Purpose of the Role

• Summarize the main purpose of the 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

• List the main responsibilities this role regularly performs. 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.

The base pay for this position is
N/A
In specific locations, the pay range may vary from the range posted.

## JOB FAMILY:
Medical & Scientific Affairs

## DIVISION:
EPD Established Pharma

## LOCATION:
India > New Delhi : New Friends Colony

ADDITIONAL LOCATIONS:

## WORK SHIFT:
Standard

## TRAVEL:
Not specified

## MEDICAL SURVEILLANCE:
Not Applicable

## SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)