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Regional Medical Affairs Specialist

Abbott
Abbott
7+ years
₹15,00,000 – ₹25,00,000 per year
Mumbai, India
10 March 11, 2026
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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 Affairs Specialist – Mumbai

A leading healthcare organization is hiring a Regional Medical Affairs Specialist in Mumbai, India to support its medical affairs strategy, clinical research activities, and regulatory collaboration. In this role, you will contribute to clinical trial execution, medical data analysis, investigator coordination, and regulatory reporting for pharmaceutical products. You will work closely with clinical investigators, regulatory teams, and medical affairs leadership to ensure that clinical studies and medical programs are conducted according to protocols and regulatory standards. This position is ideal for professionals with strong experience in medical affairs, clinical research management, and pharmaceutical product development. The estimated salary for this role ranges from ₹15 LPA to ₹25 LPA depending on experience in medical affairs and clinical research leadership.

Key Responsibilities

  • Support the planning, direction, and execution of medical affairs programs and clinical research activities.

  • Oversee clinical trial operations including Phase III and Phase IV studies for pharmaceutical products.

  • Assist in implementation of clinical protocols and completion of study reports.

  • Recruit and coordinate clinical investigators and research teams.

  • Participate in study design discussions and clinical trial cost negotiations.

  • Monitor adherence to clinical protocols and ensure timely study completion.

  • Contribute to adverse event monitoring and pharmacovigilance reporting activities.

  • Prepare and coordinate clinical research reports for submission to regulatory authorities.

  • Support investigator meetings, site initiation activities, and collaborative research programs.

  • Act as a medical liaison with external partners and organizations when required.

Required Qualifications

  • Associate’s degree or higher in Life Sciences, Pharmacy, Medicine, or related field.

  • Minimum 7 years of experience in medical affairs, clinical research, or pharmaceutical development.

  • Strong knowledge of clinical trial processes, regulatory compliance, and medical research protocols.

Required Skills

  • Medical Affairs & Clinical Research Management

  • Clinical Trial Operations (Phase III & IV)

  • Regulatory Reporting & Compliance

  • Pharmacovigilance & Safety Monitoring

  • Investigator Coordination & Clinical Protocol Management

  • Data Analysis & Medical Documentation

  • Stakeholder Communication & Collaboration

Salary

Approximate Salary: ₹15,00,000 – ₹25,00,000 per year (depending on experience in medical affairs, clinical trials, and pharmaceutical research).