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Regional Medical Advisor

Abbott
Abbott
1+ years
Not Disclosed
10 Jan. 6, 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

Regional Medical Advisor – Mumbai, India

Industry: Medical & Clinical Affairs | Location: Mumbai, Maharashtra, India

We are seeking an experienced Regional Medical Advisor to join our Medical and Clinical Affairs team in Mumbai. This role is ideal for a professional with expertise in medical affairs, clinical research, and investigator management, contributing to clinical trial planning, execution, and oversight with limited supervision.


Role Overview

As a Regional Medical Advisor, you will apply your medical knowledge to support clinical and regulatory activities, oversee human clinical trials, and ensure compliance with protocols and regulatory standards. You will work closely with investigators, internal teams, and external partners to advance clinical programs and maintain high standards of medical integrity.


Key Responsibilities

  • Oversee planning, execution, and direction of clinical trials, including phases III & IV for company products under development.

  • Contribute to the implementation of clinical protocols and facilitate completion of final reports.

  • Recruit and liaise with clinical investigators, negotiate study designs, and manage study costs.

  • Monitor adherence to clinical protocols and evaluate study progress to determine completion.

  • Participate in adverse event reporting and support pharmacovigilance/safety monitoring activities.

  • Coordinate and oversee investigator initiations, multi-center studies, and group research activities.

  • Provide reporting information for submissions to regulatory agencies.

  • Act as a consultant or liaison with other organizations under licensing or collaborative agreements.


Qualifications & Experience

  • Education: Associate Degree (or equivalent) in a relevant field.

  • Experience: Minimum 1 year in medical affairs, clinical research, or related healthcare roles.

  • Strong knowledge of clinical trial execution, protocol adherence, and regulatory compliance.

  • Effective communication and collaboration skills with investigators, internal teams, and external partners.


Key Competencies

  • Clinical expertise in medical affairs and trial oversight.

  • Ability to manage human clinical trials independently or under limited supervision.

  • Understanding of adverse event reporting and pharmacovigilance principles.

  • Strong organizational, analytical, and decision-making skills.

  • Ability to liaise effectively with investigators and external partners.