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PV Jobs – Clarivate Careers
Clarivate is inviting applications for the position of Associate Pharmacovigilance Specialist, available in multiple locations under the Life Sciences & Healthcare domain. PV Jobs offer an exciting opportunity to contribute to global pharmacovigilance efforts by monitoring biomedical literature, assessing adverse events, and supporting regulatory compliance. If you are passionate about drug safety, patient health, and scientific research, Clarivate Careers provides this perfect opportunity to build a rewarding career in pharmacovigilance.
Job Details:
- Position: Associate Pharmacovigilance Specialist
- Department: Life Sciences & Healthcare
- Location: Noida, Karnataka
- Job ID: JREQ134094
- Posted Date: October 27, 2025
- Work Model: Hybrid (Monday to Friday, 12 PM – 9 PM)
- Job Type: Full-time
About the Company:
At Clarivate, we are a global leader in providing trusted insights and analytics that accelerate the pace of innovation. Our mission is to empower professionals and organizations across industries, including Life Sciences, Healthcare, and Intellectual Property, with accurate data and expert intelligence. We are committed to delivering solutions that help our partners make critical decisions, improve research outcomes, and enhance patient safety.
Educational Requirements for the Associate Pharmacovigilance Specialist Role:
- Master’s Degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.)
- Alternatively, a degree in Information Science with at least 1 year of relevant pharmacovigilance experience
- A degree in Dentistry, Physiotherapy, or Nursing (hospital-based experience preferred)
Key Responsibilities of the Associate Pharmacovigilance Specialist Role:
- Perform pharmacovigilance services including biomedical literature monitoring, adverse event assessment, and reporting.
- Conduct indexing and abstracting using strong knowledge of scientific and medical terminology.
- Review biomedical literature for case reports, studies, and specific pharmacological topics.
- Summarize and evaluate adverse event data for drug safety compliance.
- Work with commercial and client-specific biomedical literature databases.
- Ensure adherence to pharmacovigilance regulations and reporting standards.
Skills Required for the Associate Pharmacovigilance Specialist Role:
- Experience: Fresher or up to 2 years of experience in pharmacovigilance or biomedical literature review.
- Knowledge: Strong understanding of biomedical terminology, drugs, therapeutic areas, and adverse event reporting.
- Technical Skills: Experience with biomedical databases and analytical tools.
- Desirable: Certification from a professional medical writing association or experience in scientific/medical writing.
- Soft Skills: Excellent analytical ability, attention to detail, and effective communication skills.
How to Apply?
Interested candidates can visit the Clarivate Careers Portal to apply online for the Associate Pharmacovigilance Specialist position. Keep checking official job updates and alerts for more opportunities in the Life Sciences & Healthcare division.
