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.
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