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Regional Medical Advisor

1 years
Not Disclosed
10 Nov. 19, 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

Location: Chennai, India
Category: Medical and Clinical Affairs

Job Overview

The Regional Medical Advisor will function as an experienced professional within the Medical Affairs domain, working under limited supervision. The role requires strong subject-matter expertise in medical affairs and the ability to apply advanced scientific and clinical knowledge to support clinical programs, research activities, and regulatory submissions.

This position is ideal for candidates who can independently manage medical affairs activities, ensure protocol compliance, coordinate clinical studies, and support safety and regulatory processes within the organization.


Key Responsibilities

• Oversee the planning, direction, and execution of clinical trials, including research operations and data collection activities.
• Contribute to the development and implementation of clinical study protocols and support the preparation of final clinical reports.
• Recruit and engage clinical investigators while negotiating study design, timelines, and study-related costs.
• Lead and manage human clinical trials in Phases III and IV for products under development.
• Participate in safety monitoring and adverse event reporting processes.
• Coordinate and prepare documentation required for submissions to regulatory agencies.
• Ensure strict adherence to study protocols and determine study completion criteria.
• Oversee investigator-initiated studies and multi-center research programs.
• Act as a scientific consultant or liaison with partner organizations under licensing or collaboration agreements.


Qualifications

Education

• Associate Degree or equivalent qualification in Life Sciences, Pharmacy, Medicine, or related field.

Experience Required

• Minimum 1 year of professional experience in Medical Affairs, Clinical Research, or related therapeutic/scientific functions.
• Experience in clinical trial oversight, investigator engagement, and safety reporting is preferred.