Regional Medical Advisor

Abbott; India; On-site; INR 1,200,000 - 2,000,000; Part time

Job summary

Abbott in India is seeking an experienced professional to contribute within the Medical Affairs function. The role focuses on overseeing clinical trials, data collection, and the development of protocols under limited supervision.

The position involves coordinating investigators, reporting to regulatory bodies, and ensuring safety reporting and study completion, with opportunities to liaise with external partners on licensing arrangements.

Responsibilities

• Oversees direction, planning, execution of clinical trials and data collection activities.
• Contributes to implementation of clinical protocols and facilitates final reports.
• Recruits clinical investigators and negotiates study design and costs.
• Directs human clinical trials, phases III & IV for products under development.
• Participates in adverse event reporting and safety responsibilities monitoring.
• Coordinates reporting information for regulatory submissions.
• Monitors adherence to protocols and determines study completion.
• Coordinates investigator initiations and group studies.
• May participate in adverse event reporting and safety responsibilities monitoring.

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.