Associate Pharmacovigilance Specialist
Location: Multiple Locations (Hybrid)
Job Category: Life Sciences & Healthcare
Job ID: JREQ134094
Posted Date: 28 October 2025
Overview
This Associate Pharmacovigilance Specialist role is designed for individuals looking to begin or advance their career in drug safety and biomedical literature monitoring. The position focuses on identifying, evaluating, and reporting adverse events from scientific literature, supporting global pharmacovigilance compliance for pharmaceutical products.
This role offers a strong foundation in PV operations, exposure to global safety regulations, and the opportunity to work with advanced biomedical literature databases.
Experience Required
Fresher eligible (0 years).
Candidates with up to 2 years of experience in biomedical literature review, pharmacovigilance, or drug safety will be considered an added advantage.
Key Responsibilities
Screen and evaluate biomedical literature to identify safety information related to pharmaceutical products.
Assess and summarize adverse events for regulatory submissions in alignment with international pharmacovigilance guidelines.
Conduct regular literature reviews to ensure all relevant safety cases are captured and processed.
Maintain accuracy and compliance while working with commercial or client-specific biomedical databases.
Collaborate with team members to support timely reporting, indexing, and abstracting of safety-related information.
Required Qualifications
Master’s Degree in Life Sciences, Health, or Biomedical Sciences
(Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.).
Strong knowledge of biomedical terminology, pharmacology, and therapeutic areas.
Analytical ability to interpret clinical case reports and scientific studies.
Familiarity with biomedical literature databases (commercial or client-specific).
Preferred Skills (Good to Have)
Certification in scientific or medical writing.
Exposure to drug safety or prior pharmacovigilance processes.
Experience in reviewing biomedical literature for adverse event reporting.
Background in Dentistry, Physiotherapy, or Nursing with hospital-based clinical exposure.
Strong written communication and summarization skills.
About the Team
The Pharmacovigilance unit consists of professionals across India working under experienced team managers. The team brings strong competence in healthcare analytics, market research, and safety monitoring within the life sciences domain.
Work Schedule
Work Hours: 12:00 PM to 9:00 PM
Work Mode: Hybrid
Equal Opportunity Statement
Clarivate is committed to fair and equal employment opportunities. All qualified applicants will receive consideration without discrimination in hiring, compensation, promotion, or training, in accordance with applicable laws and regulations across global locations.
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