Full Time

Medical Reviewer - Pharmacovigilance

Latinum HR Solutions
India
Salary Not Disclosed
Posted 10/03/2026

About the Role

Why This Role Matters

Medical reviewers in pharmacovigilance play a crucial role in ensuring drug safety by evaluating adverse event reports and determining their medical significance. Their work helps pharmaceutical companies comply with regulatory standards and ensures that medicines remain safe and effective for patients worldwide.

Job Description

Latinum HR Solutions is hiring a Medical Reviewer – Pharmacovigilance for a leading Life Sciences organization. This is a non-clinical, full-time role suitable for doctors who want to build a long-term career in drug safety and pharmacovigilance. The role focuses on reviewing Individual Case Safety Reports (ICSRs) in global safety databases and evaluating the medical relevance and causality of reported adverse events.

Key Features of the Role

• Position: Medical Reviewer – Pharmacovigilance
• Company: Latinum HR Solutions
• Location: Mumbai, Pune, Bangalore, Chennai, Indore, India
• Industry: Life Sciences / Pharmacovigilance / Drug Safety
• Employment Type: Full-Time
• Work Mode: Work from Office
• Experience Required: 3+ Years

Responsibilities

• Perform medical review of clinical, spontaneous, solicited, and literature adverse event cases
• Assess seriousness, causality, labeling, and medical accuracy of safety cases
• Review narratives, adverse event terms, suspect drugs, concomitant medications, lab data, and medical history
• Evaluate Individual Case Safety Reports (ICSRs) in global safety databases
• Ensure compliance with global and local regulatory guidelines and SOP timelines
• Provide medical input and product-related guidance to drug safety teams
• Generate, send, and track medical follow-up queries for safety cases
• Respond to case-related queries within the safety database
• Support audits, internal reviews, and client discussions
• Provide medical input for SUSAR and other critical safety cases

Required Qualification

• MBBS or equivalent medical degree (Mandatory)

Important Requirements

• Minimum 3+ years of experience in pharmacovigilance, drug safety, or life sciences domain
• Strong medical and clinical knowledge
• Understanding of pharmacovigilance and drug safety processes
• Computer proficiency including MS Office and safety databases
• Excellent written and verbal communication skills
• Ability to work effectively in a multidisciplinary team environment
• Strong attention to detail and problem-solving ability

What We Offer

• Opportunity to build a long-term career in pharmacovigilance
• Exposure to global drug safety processes
• Collaborative work environment within life sciences organizations

Experience and Skills

• Pharmacovigilance and drug safety case review
• Medical evaluation of adverse events
• Clinical knowledge and decision making
• Regulatory compliance and SOP adherence
• Communication and teamwork

Company Overview

Latinum HR Solutions is a recruitment and talent acquisition firm specializing in hiring professionals for the life sciences, pharmaceutical, biotechnology, and healthcare industries. The company partners with leading organizations to recruit skilled professionals in pharmacovigilance, drug safety, and other specialized healthcare roles.

FAQs

  1. What qualification is required for this role?
    Candidates must have an MBBS or equivalent medical degree.

  2. How much experience is required?
    A minimum of 3 years of experience in pharmacovigilance or drug safety is required.

  3. Is this a clinical or non-clinical role?
    This is a non-clinical role focused on pharmacovigilance and drug safety review.

  4. Where is the job located?
    The role is available in Mumbai, Pune, Bangalore, Chennai, and Indore.

Application Tips

• Highlight your MBBS qualification and pharmacovigilance experience
• Mention experience in ICSR review and adverse event assessment
• Showcase knowledge of drug safety databases and regulatory guidelines
• Emphasize analytical skills and medical judgment

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