Regional Medical Advisor
Abbott · Delhi
- Experience2–7 yrs
- SalaryNot disclosed
- Work modeonsite
- Levelsenior
- Posted14 Sept 2026
About Abbott
Abbott is hiring in Delhi in healthcare. This role looks for around 2+ years of experience.
Skills
- Medical Affairs
- clinical trials
- clinical research
- clinical protocols
- adverse event reporting
- regulatory reporting
- clinical investigators
- study design
- clinical safety
- regulatory agencies
The role
A clinical research advisor at a healthcare products company directs clinical trials and applies Medical Affairs expertise to clinical protocols and adverse event reporting. The role coordinates regulatory reporting and investigator studies.
Full 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.