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Regional Medical Advisor

1+ years
Not Disclosed
10 Nov. 11, 2025
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

Location: Chennai, India
Category: Medical and Clinical Affairs


Role Summary

Experienced professional individual contributor in Medical Affairs, applying subject matter expertise to support clinical trials, research, and medical data activities. Works under limited supervision and adapts knowledge to meet specific study and organizational needs.


Key Responsibilities

1. Clinical Trial Oversight

  • Directs and oversees human clinical trials (Phase III & IV) for company products under development.

  • Contributes to implementation of clinical protocols and facilitates completion of final study reports.

  • Monitors adherence to protocols and determines study completion.

  • Coordinates and oversees investigator initiations and group studies.

2. Investigator & Study Management

  • Recruits clinical investigators and negotiates study designs and costs.

  • Coordinates reporting of trial data for submission to regulatory agencies.

  • Acts as consultant or liaison with other organizations under licensing agreements (if applicable).

3. Safety & Regulatory Support

  • Participates in adverse event reporting and monitors safety responsibilities.

  • Provides support for regulatory reporting and compliance documentation.


Qualifications

Education

Field / Level

Associates Degree

±13 years or equivalent in relevant field

Experience

Details

Minimum 1 year

Experience in Medical Affairs, clinical trials, or related field


Core Competencies

  • Clinical Trial Management (Phase III & IV)

  • Protocol Implementation & Study Oversight

  • Investigator Recruitment & Study Coordination

  • Safety & Adverse Event Monitoring

  • Regulatory Reporting & Compliance

  • Cross-functional Collaboration