💊 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
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