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.

u2022As the Experienced skilled in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.

u2022Contributes to implementation of clinical protocols, and facilitates completion of final reports.

u2022Recruits clinical investigators and negotiates study design and costs.

u2022Responsible for directing human clinical trials, phases III & IV for company products under development.





u2022Participates in adverse event reporting and safety responsibilities monitoring.

u2022Coordinates and provides reporting information for reports submitted to the regulatory agencies.

u2022Monitors adherence to protocols and determines study completion.

u2022Coordinates and oversees investigator initiations and group studies.

u2022May participate in adverse event reporting and safety responsibilities monitoring.

u2022May act as consultant/liaison with other corporations when working under licensing agreements.

Freshers or Minimum 1 year experience

📌 Regional Medical Advisor (Kolkata)
🏢 Abbott Vascular
📍 Kolkata