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Regional Medical Affairs Specialist

Abbott
Abbott
7+ years
Not Disclosed
Mumbai, India
1 May 7, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills:

Regional Medical Affairs Specialist – Clinical Research & Medical Affairs Job in Mumbai, India

Company: Abbott Laboratories
Job Title: Regional Medical Affairs Specialist
Location: Mumbai, India
Department: Medical and Clinical Affairs
Job Type: Full-Time


About Abbott

Abbott is a globally recognized healthcare and pharmaceutical organization committed to improving patient outcomes through innovative medicines, diagnostics, nutrition solutions, and medical technologies. With a strong global presence, Abbott continues to advance healthcare through scientific research, clinical development, and medical affairs excellence.


Job Overview

Abbott is hiring a highly experienced Regional Medical Affairs Specialist to join its Medical and Clinical Affairs team in Mumbai, India. This role is designed for senior medical affairs professionals with extensive experience in clinical research, clinical trial management, investigator coordination, and regulatory support activities.

The selected candidate will oversee complex clinical programs, support the execution of Phase III and Phase IV clinical trials, contribute to medical strategy, and collaborate with regulatory agencies and external investigators. The role also includes safety monitoring, protocol management, and cross-functional scientific collaboration.

This position offers an excellent opportunity for experienced healthcare and pharmaceutical professionals seeking senior-level careers in medical affairs and clinical development.


Experience Required

Experience Level

  • Senior-Level Medical Affairs Professional
  • Freshers are not eligible

Required Experience

  • Minimum 7 years of experience in:
    • Medical Affairs
    • Clinical Research
    • Clinical Trial Operations
    • Pharmaceutical Industry
    • Healthcare Research Programs

Preferred Expertise

  • Phase III & IV Clinical Trials
  • Clinical Protocol Management
  • Investigator Coordination
  • Regulatory Reporting
  • Adverse Event Monitoring
  • Medical Affairs Strategy

Educational Qualification

Required Qualification

  • Associate Degree or equivalent qualification in:
    • Life Sciences
    • Pharmacy
    • Medicine
    • Clinical Research
    • Healthcare-related discipline