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Regional Medical Advisor

1-3 years
Not Disclosed
10 Nov. 20, 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
Department: Medical and Clinical Affairs
Experience Required: Minimum 1–3 years in Medical Affairs, Clinical Research, or related therapeutic functions

Job Overview

ThePharmaDaily.com is seeking a Regional Medical Advisor to support medical and clinical affairs activities within regional operations. This role is designed for an experienced professional contributor with a strong background in Medical Affairs, clinical research processes, and protocol implementation. The position requires the ability to work independently while applying technical and scientific knowledge to support medical strategy, clinical studies, and regulatory reporting.

Main Purpose of the Role

  • Serve as an experienced Medical Affairs professional working under limited supervision.

  • Apply medical and scientific knowledge to support clinical programs and regional medical initiatives.

  • Utilize domain expertise to address operational needs and ensure alignment with medical and regulatory requirements.

Key Responsibilities

Clinical Research and Trial Management

  • Oversee planning, execution, and data collection activities for clinical research and Phase III and IV clinical trials.

  • Support the development and implementation of clinical protocols and assist in the preparation of final study reports.

  • Recruit and manage clinical investigators, including negotiation of study design, timelines, and costs.

  • Monitor adherence to clinical trial protocols and determine study completion status.

  • Coordinate investigator-initiated studies and multi-center group studies.

Medical Affairs and Regulatory Support

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

  • Compile clinical and medical data required for submission to regulatory authorities.

  • Serve as a liaison with external partners or collaborating organizations involved in licensed research or clinical programs.

  • Provide scientific guidance and ensure alignment of clinical activities with corporate medical strategies.

Qualifications

Education

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

  • Higher qualifications are preferred.

Experience

  • Minimum 1 year of experience in Medical Affairs, clinical research, or related operations.

  • Experience supporting clinical trials, protocol interpretation, and safety reporting is highly desirable.

  • Strong understanding of regulatory requirements and clinical research processes.