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Medical Reviewer – Vaf 372

3-4 years
₹12 LPA – ₹20 LPA
10 Aug. 5, 2025
Job Description
Job Type: Full Time Education: MBBS/MD 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

Medical Reviewer – VAF 372
Location: India (Remote Work Possible)
Department: Safety and Vigilance – Life Cycle
Job Type: Permanent Contract
Company: ProductLife Group

Estimated Salary: ₹12 LPA – ₹20 LPA (based on 3–4 years of PV experience with MBBS/MD in India)


Position Overview:

ProductLife Group is seeking experienced Medical Reviewers with 3–4 years of pharmacovigilance (PV) experience and a background in medicine (MBBS/MD) to join our dynamic Safety and Vigilance team. This role focuses on the medical review of ICSRs in post-marketing drug safety and clinical studies, contributing to safety evaluation and regulatory compliance.


Key Responsibilities:

Medical Review & Safety Assessment:

  • Perform medical review of Individual Case Safety Reports (ICSRs) from:

    • Spontaneous reports

    • Literature sources

    • Clinical studies

  • Conduct initial triage and seriousness assessment of cases.

  • Support causality assessment, medical evaluation, and benefit-risk analysis of medicinal products.

  • Perform secondary case reviews to ensure accuracy and competency.

Client & Compliance Interaction:

  • Participate in client communication, ensuring expectations are met or exceeded.

  • Represent the company during audits and inspections as required.

  • Maintain up-to-date understanding of client-specific conventions, SOPs, and regulatory standards.

Training & Mentorship:

  • Train and mentor junior team members in:

    • Good case assessment practices

    • MedDRA coding

    • Pharmacovigilance best practices


Requirements:

Educational Qualifications:

  • MBBS or MD (Doctor of Medicine) – Mandatory

Experience:

  • 3–4 years of experience in pharmacovigilance within a pharmaceutical company or service provider.

  • Prior involvement in post-marketing safety activities.

  • Familiarity with safety databases (e.g., Argus, ARISg, Veeva Vault Safety, etc.)

  • Experience in client communication and collaboration.

Additional Skills:

  • Strong written and verbal communication skills.

  • High emotional intelligence and adaptability.

  • Analytical mindset and attention to detail.

  • Strong organizational skills and punctuality.

  • Previous clinical experience is an added advantage.

  • Ability to deliver feedback constructively and mentor peers.


This is an exciting opportunity for medical professionals passionate about drug safety and risk evaluation to join a global team working at the forefront of pharmacovigilance solutions.