Senior Manager Medical Affairs

Abbott; Mumbai; On-site; INR 1,200,000 - 2,400,000; Full time

Job summary

Abbott in Mumbai, India seeks a Medical Affairs Supervisor to lead a small professional team and oversee clinical trials, data collection, and regulatory activities. The role focuses on mentoring, coaching, and coordinating diverse experts to ensure compliant study execution.

The position manages Phase III/IV trials, supports adverse event reporting, and collaborates with investigators and cross-functional teams to deliver final reports and regulatory submissions.

Qualifications

• Supervises a team of more than 2 professionals within Medical Affairs.
• First level manager with coaching and coordination responsibilities.
• Minimum 4 years of relevant experience in medical/scientific affairs.

Responsibilities

• Oversees direction, planning, and execution of clinical trials/research and data collection.
• Contributes to implementation of clinical protocols and final reports.
• Recruits clinical investigators and negotiates study design and costs.
• Directs human clinical trials, Phases III and IV for products under development.
• Participates in adverse event reporting and safety monitoring.
• Coordinates reporting for regulatory submissions and audits.
• Ensures adherence to study protocols and completion criteria.
• Liaises with other entities under licensing agreements as needed.

Skills

Team leadership

Mentoring

Coaching

Coordination

Education

Associates Degree (13 years)

Job description

JOB DESCRIPTION

MAIN PURPOSE OF THE ROLE

Leads/supervises a team of more than 2 professionals within the Medical Affairs Sub-Function.

First level manager of a work team that may comprise professionals, technical and/or administrative staff.

Typically without budget or hire/fire authority.

Focuses on mentoring, coaching, and coordination.

MAIN RESPONSIBILITIES

• As the Supervisor of the Medical Affairs Sub-Function, supervises professionals 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 Level Major/Field of Study or Equivalent

• Associates Degree ( 13 years)

Experience/Background

• Minimum 4 years

The base pay for this position is

N/A

In specific locations, the pay range may vary from the range posted.

JOB FAMILY: Medical & Scientific Affairs

DIVISION: EPD Established Pharma

LOCATION: India > Mumbai : BKC Building

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)

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.