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Associate Pharmacovigilance Specialist

2 years
Not Disclosed
10 Nov. 17, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Job Title: Associate Pharmacovigilance Specialist

Job Type: Full-Time
Work Mode: Hybrid
Locations:

  • R271 – Noida

  • IND – Bangalore (DRG)
    Posted: 20 Days Ago
    Requisition ID: JREQ134094


Role Overview

The Associate Pharmacovigilance Specialist is responsible for monitoring biomedical literature to identify and assess adverse events for regulatory reporting. The role requires strong understanding of scientific and medical terminology, pharmacovigilance regulations, and experience with biomedical literature databases.


Key Responsibilities

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

  • Assess adverse events and ensure compliance with pharmacovigilance regulatory reporting requirements.

  • Conduct routine literature reviews to capture and report potential adverse events.

  • Summarize key points from biomedical case reports, studies, and scientific topics.


Required Education, Experience & Skills

Education

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

Experience

  • Fresher to 2 years experience in reviewing biomedical literature for adverse event reporting
    OR equivalent experience (e.g., information science degree + 1 year relevant experience).

  • Experience in drug safety/pharmacovigilance is desirable.

Skills

  • Strong analytical skills for summarizing biomedical content.

  • Working knowledge of biomedical terminology, drugs, and therapeutic areas.

  • Experience with commercial and client-specific biomedical literature databases.


Preferred / Good-to-Have Qualifications

  • Certification from a professional medical writing association.

  • Background in scientific or medical writing.

  • Degree in Dentistry, Physiotherapy, or Nursing with hospital-based patient exposure.

  • Additional experience with biomedical literature databases.


About the Team

The Pharmacovigilance team is based across India and consists of professionals reporting to regional team managers. The team brings extensive experience in market research and consulting, particularly in medical devices and healthcare.


Work Hours

  • Shift: 12:00 PM to 9:00 PM IST (Regular working hours)