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Regional Medical Advisor

3-7 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 – Chennai, India

Category: Medical and Clinical Affairs

Role Overview

The Regional Medical Advisor is an experienced individual contributor role within Medical Affairs, responsible for providing scientific expertise and ensuring high-quality execution of clinical and medical projects. This position operates with limited supervision and requires strong subject-matter knowledge to support clinical strategy, trial execution, and regulatory-aligned activities across assigned therapeutic areas.

The ideal candidate should demonstrate the ability to apply medical and clinical knowledge to meet specific organizational and research needs.


Key Responsibilities

Clinical and Research Leadership

  • Oversee the planning, direction, and execution of clinical trials and research activities, ensuring quality, accuracy, and timely data collection.

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

Clinical Trial Oversight

  • Recruit and engage clinical investigators while negotiating study design parameters and cost considerations.

  • Lead and manage Phase III and Phase IV clinical studies for products under development.

  • Review study progress, monitor adherence to protocols, and determine study completion criteria.

Safety and Regulatory Support

  • Participate in adverse event reporting, safety monitoring, and adherence to safety standards.

  • Coordinate and submit scientific and clinical documentation required for regulatory reporting.

Stakeholder Coordination

  • Manage investigator-initiated research and collaborative group studies.

  • Act as a scientific consultant or liaison with partner organizations during licensing or co-development activities.


Qualifications and Experience Required

  • Minimum Associate Degree or equivalent (approximately 13 years of formal education).

  • 3–7 years of experience in Medical Affairs, Clinical Research, or related scientific functions is preferred.

  • Experience in conducting or supporting Phase III and Phase IV clinical trials is highly desirable.

  • Strong understanding of clinical protocol development, investigator management, and regulatory compliance.

  • Familiarity with adverse event reporting and clinical safety processes.

  • Ability to work independently, manage multiple stakeholders, and collaborate effectively across functional teams.


Location

Chennai, India