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Associate Pharmacovigilance Specialist

2+ years
Not Disclosed
10 Nov. 12, 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

Job ID:

JREQ134094

Posted Date:

October 28, 2025

Location:

Available in 2 locations – Remote/Hybrid

Department:

Life Sciences & Healthcare


🧬 Role Overview

The Associate Pharmacovigilance Specialist is responsible for performing pharmacovigilance activities including:

  • Biomedical literature monitoring

  • Assessing adverse events for regulatory reporting

  • Indexing and abstracting safety data

The role requires a solid understanding of scientific terms, medical terminology, drugs, therapeutic areas, and pharmacovigilance regulations.


🎓 Education & Experience Requirements

Essential:

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

  • Fresher or up to 2 years of experience in reviewing biomedical literature for adverse event reporting OR an equivalent combination of education and experience (e.g., Information Science degree + 1 year relevant experience in drug/patient safety)

  • Familiarity with pharmacovigilance and drug safety processes

Desirable:

  • Prior experience in drug safety/pharmacovigilance

  • Strong analytical skills to summarize biomedical case reports, studies, or specific topics

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

  • Experience with commercial and client-specific biomedical literature databases

Additional Advantage:

  • Certification from a professional medical writer’s association

  • Scientific/medical writing background

  • Degrees in Dentistry, Physiotherapy, Nursing with patient exposure


⚙️ Key Responsibilities

  • Screen biomedical literature to identify safety information of pharmaceutical products

  • Assess adverse events for regulatory reporting in compliance with pharmacovigilance regulations

  • Conduct regular literature reviews to ensure all relevant adverse event cases are captured and reported

  • Maintain accurate documentation of findings in accordance with internal SOPs and regulatory guidelines


👥 About the Team

  • Part of the Pharmacovigilance team across India

  • Team comprises professionals reporting to respective team managers

  • Focused on market research and consulting within medical devices and healthcare sectors


Work Hours & Mode

  • Working Hours: 12:00 PM – 9:00 PM

  • Work Mode: Hybrid


🌟 Why Join Clarivate

  • Equal employment opportunities for all qualified candidates

  • Commitment to non-discrimination in hiring, compensation, promotion, training, and other employment terms

  • Compliance with all applicable local and international employment laws and regulations