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Associate Pharmacovigilance Specialist

0-2 years
Not Disclosed
10 Nov. 6, 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

Job Title: Associate Pharmacovigilance Specialist

Company: Clarivate
Job ID: JREQ134094
Posted Date: October 28, 2025
Category: Life Sciences & Healthcare
Work Mode: Hybrid
Locations: Bangalore / Noida, India


Job Summary

The Associate Pharmacovigilance Specialist performs pharmacovigilance services such as biomedical literature monitoring, adverse event identification, indexing, and abstracting. The role requires strong knowledge of biomedical terminology, drugs, therapeutic areas, and pharmacovigilance regulations.


Key Responsibilities

  • Screen biomedical literature to identify and assess safety information of pharmaceutical products.

  • Evaluate potential adverse events for regulatory reporting in compliance with pharmacovigilance guidelines.

  • Conduct literature reviews to capture and report relevant safety cases.

  • Ensure accuracy and consistency in summarizing scientific data and case reports.


Education, Experience, and Skills

Required:

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

  • Fresher or up to 2 years of experience in reviewing biomedical literature for adverse event reporting OR equivalent education and experience (e.g., Information Science degree with at least 1 year of relevant experience).

  • Related experience in Drug Safety/Pharmacovigilance is desirable.

  • Strong analytical ability to summarize key findings from biomedical literature.

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

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

Preferred:

  • Certification from a professional medical writing association.

  • Experience with scientific/medical writing.

  • Degree in Dentistry, Physiotherapy, or Nursing (with hospital exposure).


About the Team

The Pharmacovigilance team at Clarivate consists of professionals based across India, each reporting to their respective team managers. The team combines strong expertise in market research, consulting, medical devices, and healthcare sectors.


Work Schedule

  • Regular Hours: 12:00 PM – 9:00 PM IST

  • Work Mode: Hybrid


Equal Opportunity Statement

At Clarivate, we are committed to providing equal employment opportunities for all qualified persons in all employment-related aspects including hiring, compensation, training, and advancement. We comply with all applicable laws and regulations governing non-discrimination.