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Regional Medical Advisor

5-12 years
Not Disclosed
10 Dec. 11, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Regional Medical Advisor – Mumbai, India

Full-Time | Medical & Scientific Affairs | EPD Division
Experience Required: 5–12 Years
Job ID: 31134675

About the Role

The Regional Medical Advisor is an experienced individual contributor responsible for supporting Medical Affairs activities with limited supervision. The role requires strong subject-matter expertise in clinical research, medical affairs strategy, and regulatory alignment. The position involves applying advanced knowledge to meet organizational and regional medical needs.

Key Responsibilities

  • Lead and oversee activities related to clinical trial planning, execution, monitoring, and data collection in alignment with Medical Affairs objectives.

  • Support the implementation of clinical protocols and contribute to the preparation and completion of final clinical study reports.

  • Recruit, engage, and coordinate with clinical investigators while negotiating study designs, timelines, and budget requirements.

  • Manage human clinical trials (Phases III & IV) for assigned products under development.

  • Participate in adverse event monitoring, safety review activities, and reporting processes.

  • Coordinate data and documentation required for submission to regulatory authorities.

  • Monitor protocol adherence, study timelines, and overall trial progress to ensure compliance and timely completion.

  • Oversee investigator-initiated studies and collaborative research programs.

  • Serve as a scientific consultant or liaison for partnered corporate organizations under licensing agreements.

Required Experience & Qualifications

  • 5–12 years of experience in Medical Affairs, Clinical Research, or related medical/scientific roles.

  • Strong understanding of clinical trial processes, regulatory guidelines, and safety reporting.

  • Proven ability to collaborate with investigators, research teams, and cross-functional stakeholders.

  • Experience contributing to Phases III & IV clinical studies.

  • Strong verbal and written communication skills with the ability to interpret and present scientific data.

  • Ability to work independently and manage multiple medical affairs initiatives.

Work Conditions

  • Location: BKC Building, Mumbai, India

  • Work Type: Full-time

  • Shift: Standard

  • Travel: As required (not specified)

  • Physical Requirements: Ability to sit continuously for extended periods.

About the Division

This position is part of the Established Pharma Division (EPD), supporting medical and scientific operations that drive product development, safety, and post-market clinical initiatives.

Compensation

Base pay is not disclosed in this posting. Compensation may vary based on location and company policy.a