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Regional Medical Advisor

5-8 years
Not Disclosed
10 Dec. 8, 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

Category: Medical and Clinical Affairs

About the Role

The Regional Medical Advisor is a key individual contributor role within Medical Affairs, supporting scientific, clinical, and evidence-based activities across assigned therapeutic areas. This position requires an experienced professional capable of independently applying medical and clinical expertise to advance clinical programs, research initiatives, and regulatory-aligned activities.

This role operates under limited supervision and demands strong analytical, scientific, and stakeholder-engagement capabilities. The ideal candidate will contribute significantly to clinical strategy, protocol implementation, and data-driven medical decision-making.


Key Responsibilities

The Regional Medical Advisor will be responsible for the following core activities:

Clinical and Medical Affairs Leadership

  • Provide scientific and medical expertise within the Medical Affairs function, ensuring alignment with clinical and regulatory standards.

  • Oversee planning, execution, and monitoring of clinical trials (Phases III and IV), research programs, and data-collection initiatives.

  • Support the development, implementation, and completion of clinical protocols and final study reports.

Clinical Study Management

  • Recruit and engage clinical investigators while negotiating study design, scope, and budgets.

  • Monitor adherence to study protocols, manage study timelines, and assess criteria for study completion.

  • Coordinate and supervise investigator-initiated studies and group research projects.

Safety and Compliance

  • Participate in adverse event reporting and safety monitoring activities, ensuring compliance with national and international standards.

  • Coordinate relevant safety and regulatory documentation for submission to governing authorities.

Cross-Functional Collaboration

  • Act as a medical consultant or liaison with partner organizations, particularly within licensing or collaborative agreements.

  • Provide scientific input to internal teams to ensure consistent and accurate communication of clinical insights.


Experience Required

  • Minimum 5–8 years of experience in Medical Affairs, Clinical Research, or related scientific functions.

  • Prior experience managing clinical trials (Phase III/IV) is strongly preferred.

  • Demonstrated expertise in clinical protocol development, investigator management, and safety reporting.

  • Strong understanding of regulatory processes and medical compliance frameworks.

  • Experience collaborating with cross-functional teams and external investigators.


Competencies and Skills

  • Excellent knowledge of clinical research methodologies and Good Clinical Practice (GCP).

  • Strong communication and scientific presentation skills.

  • Ability to analyze clinical data and contribute to evidence-based decision-making.

  • Capability to build strong relationships with investigators, clinicians, and regulatory partners.

  • Ability to work independently with minimal supervision.


Work Location

Mumbai, India