Instagram
youtube
Facebook

Associate Pharmacovigilance Specialist

0-2 years
Not Disclosed
10 Nov. 14, 2025
Job Description
Job Type: Full Time Hybrid 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

Associate Pharmacovigilance Specialist – Structured Job Description

Job ID: JREQ134094
Locations: 2 (Hybrid)
Department: Life Sciences & Healthcare
Posted on: October 28th, 2025
Work Mode: Hybrid
Work Hours: 12:00 PM – 9:00 PM


1. Role Summary

The Associate Pharmacovigilance Specialist is responsible for monitoring biomedical literature, identifying adverse events, and performing safety assessment for regulatory reporting. The role requires strong scientific knowledge, analytical skills, and familiarity with pharmacovigilance regulations and terminology.


2. Key Responsibilities

A. Literature Screening & Safety Case Identification

  • Screen biomedical literature for safety information related to pharmaceutical products.

  • Identify and assess adverse events in compliance with PV regulatory requirements.

  • Conduct regular literature reviews to capture potential safety cases.

B. Adverse Event Assessment

  • Analyze findings and determine cases relevant for regulatory reporting.

  • Summarize and index biomedical case reports, studies, and topic-specific content.

C. Documentation & Compliance

  • Ensure all identified cases meet regulatory submission requirements.

  • Maintain compliance with global pharmacovigilance standards and internal procedures.


3. Required Qualifications

Education

  • Master’s Degree in Life Sciences, Health, or Biomedical Sciences
    (e.g., Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.)

Experience

  • Fresher to 2 years experience in biomedical literature review or PV-related work

  • OR an equivalent combination (e.g., Information Science degree with ≥1 year relevant experience)

Skills

  • Strong analytical ability to evaluate and summarize biomedical literature

  • Knowledge of medical terminology, drugs, and therapeutic areas

  • Familiarity with PV regulations

  • Experience using commercial or client-specific biomedical literature databases


4. Preferred Qualifications

  • Certification from a professional medical writing association

  • Scientific/medical writing experience

  • Experience with biomedical literature databases

  • Degree with clinical exposure (Dentistry, Nursing, Physiotherapy)


5. About the Team

A distributed Pharmacovigilance team based across India, reporting to respective team managers.
The team brings strong market research and medical/healthcare consulting expertise.


6. Work Environment

  • Mode: Hybrid

  • Working Hours: 12:00 PM – 9:00 PM

  • Equal opportunity employer; follows global non-discrimination standards.