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Job Description
Job Title: Associate, Pharmacovigilance Specialist
Location: Hybrid (Monday to Friday)
Company: Clarivate
Job Type: Full-time
Introduction
The Associate Pharmacovigilance Specialist is responsible for performing key pharmacovigilance (PV) services, including biomedical literature monitoring, adverse event assessment, indexing, and abstracting.
The role demands strong scientific knowledge, familiarity with PV regulations, and proficiency in medical terminology and therapeutic domains. This position directly supports global drug safety processes and ensures compliance with regulatory standards.
Role & Responsibilities
- Monitor biomedical literature for adverse events and potential safety signals.
- Evaluate and summarize key findings from published case reports, studies, and scientific papers.
- Conduct indexing and abstracting activities based on standardized PV protocols.
- Maintain high accuracy and compliance with pharmacovigilance regulations and client-specific requirements.
- Work collaboratively with global teams to ensure timely and quality delivery of reports.
- Adapt to evolving project requirements and contribute to process improvement initiatives.
Educational Qualification
- Master’s Degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.)
- A degree in Dentistry, Physiotherapy, or Nursing (with hospital exposure) is an added advantage.
Experience:
- 1–2 years of experience reviewing biomedical literature for adverse event reporting OR equivalent experience in pharmacovigilance or drug safety.
- Prior experience in drug safety, scientific writing, or medical information analysis is desirable.
Location
Hybrid (Monday to Friday)
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