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Main Purpose of the Role

- Summarize the main purpose of the roleExperienced 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/AIn specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Medical & Scientific Affairs

DIVISION:

EPD Established Pharma

LOCATION:

India > New Delhi : Recent 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)

📌 Regional Medical Advisor (New Delhi)
🏢 Abbott
📍 New Delhi