Senior Medical Advisor

Abbott; Mumbai; On-site; INR 1,500,000 - 2,700,000; Full time

Job summary

Abbott is seeking a highly experienced Specialist in the Medical Affairs Sub-Function to oversee direction, planning, execution of clinical trials, and comprehensive data collection activities.

The role includes contributing to clinical protocol implementation, final reporting, and coordination with regulatory agencies. Responsibilities extend to recruiting investigators, negotiating study designs and costs, and directing Phase III & IV trials for products under development.

Qualifications

• Education level: Associates Degree (± 13 years) or equivalent.

Responsibilities

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

Education

Associates Degree (± 13 years)

Job description

Job Description:

Main Responsibilities

• As the Specialist in the Medical Affairs Sub-Function, considered as highly experienced and knowledgeable resource within the organization 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.

Qualifications

Education

Education Level

Major/Field of Study

or

Equivalent

Associates Degree (± 13 years)

Experience/Background

Experience

Experience Details

Minimum 7 years

Licenses and Certifications

Language Proficiency

Language

Proficiency

Requirements: