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Regional Medical Advisor

Abbott
Abbott
1-3 years
Not Disclosed
10 Jan. 21, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Regional Medical Advisor
Location: Mumbai, India
Category: Medical & Clinical Affairs
Experience Required: Minimum 1–3 years in Medical Affairs, Clinical Research, or Pharmaceutical Industry

Job Overview:
We are seeking an experienced Regional Medical Advisor to support our Medical Affairs team in Mumbai. This role is ideal for a skilled professional who works independently under limited supervision, applies scientific expertise in medical affairs, and contributes to clinical research and regulatory compliance. The candidate will play a key role in executing clinical trials, managing study protocols, and providing strategic medical insights to support company products and initiatives.

Key Responsibilities:

  • Apply subject matter expertise in Medical Affairs to plan, execute, and oversee clinical trials and research activities.

  • Contribute to the development and implementation of clinical study protocols and ensure completion of final reports.

  • Recruit and manage clinical investigators, negotiate study designs, and oversee budgeting for clinical trials.

  • Direct human clinical trials (Phases III & IV) for products under development, ensuring high-quality data collection and compliance.

  • Monitor adherence to protocols, track study progress, and determine study completion.

  • Coordinate investigator initiations, group studies, and cross-functional collaborations as required.

  • Participate in adverse event reporting, safety monitoring, and regulatory compliance activities.

  • Act as a consultant or liaison with external organizations or partners under licensing agreements when required.

  • Provide accurate and timely reporting to regulatory agencies as per company and local requirements.

Qualifications & Experience:

  • Bachelor’s degree in Pharmacy, Life Sciences, Medicine, or a related field.

  • Minimum 1–3 years of experience in Medical Affairs, Clinical Research, or Pharmaceutical Industry.

  • Hands-on experience in clinical trial management, protocol development, and investigator coordination.

  • Strong knowledge of adverse event reporting, safety monitoring, and regulatory compliance.

  • Excellent communication, organizational, and stakeholder management skills.

  • Ability to work independently while collaborating effectively with cross-functional teams.

Why Join Us:

  • Be part of a globally recognized pharmaceutical organization driving clinical excellence.

  • Work in a dynamic environment contributing to impactful medical and clinical initiatives.

  • Gain exposure to advanced clinical research and regulatory processes.

Apply Today to advance your career as a Regional Medical Advisor and make a meaningful impact in medical affairs and clinical research.