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Medical Review Specialist – Drug Safety & Pharmacovigilance

Vizen Life Sciences
Vizen Life Sciences
0-5 years
Not Disclosed
Hyderabad
1 May 8, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development

Medical Review Specialist – Drug Safety & Pharmacovigilance
Location: Hyderabad
Company: Vizen Life Sciences
Job Type: Full-Time
Work Mode: Work From Office (Mandatory)
Industry: Pharmacovigilance / Drug Safety / Clinical Research


About the Company

Vizen Life Sciences is a growing healthcare and life sciences organization focused on delivering high-quality pharmacovigilance, drug safety, and medical review solutions for pharmaceutical and healthcare clients. The company is committed to maintaining global safety standards, regulatory compliance, and patient-focused healthcare services.


Job Overview

Vizen Life Sciences is hiring skilled and detail-oriented professionals for the role of Medical Review Specialist – Drug Safety & Pharmacovigilance. The selected candidate will be responsible for medical review, safety analysis, aggregate reporting, and pharmacovigilance assessment activities related to Individual Case Safety Reports (ICSRs) and aggregate safety reports.

This role is ideal for candidates with strong expertise in drug safety, medical review, pharmacovigilance operations, and regulatory compliance within pharmaceutical, CRO, or healthcare environments.


Role Details

  • Designation: Drug Safety Physician / Medical Review Specialist
  • Department: Pharmacovigilance & Drug Safety
  • Experience Required: 0–5 Years
  • Qualification: MBBS / MD in Pharmacology
  • Joining Preference: Immediate Joiners Preferred

Key Responsibilities

  • Provide medical review, analysis, and guidance during the case handling and reporting cycle of:
    • Individual Case Safety Reports (ICSRs)
    • ADR reports for investigational and marketed products
  • Conduct detailed ICSR medical review to assess:
    • Causality
    • Seriousness
    • Completeness
    • Regulatory compliance
  • Prepare and review:
    • Aggregate safety reports
    • PSURs (Periodic Safety Update Reports)
    • PADERs (Periodic Adverse Drug Experience Reports)
  • Perform safety surveillance and signal detection activities
  • Analyze adverse drug events (ADEs) and identify potential safety risks
  • Provide guidance to Drug Safety Associates on:
    • Medical safety assessments
    • Aggregate data analysis
    • Case-by-case evaluation
  • Participate in:
    • Safety Review Meetings
    • Client discussions
    • Regulatory review discussions
  • Support internal audits and regulatory inspection readiness activities
  • Ensure compliance with global pharmacovigilance regulations and safety standards

Required Qualifications

Candidates must possess any of the following qualifications:

  • MBBS
  • MD in Pharmacology

Experience Requirements

  • 0 to 5 years of experience in:
    • Pharmacovigilance
    • Drug safety
    • Medical review
    • Clinical research
  • Freshers with relevant qualifications and strong pharmacovigilance knowledge may also apply