Position: Associate Pharmacovigilance Specialist
Department: Life Sciences & Healthcare
Job ID: JREQ134094
Locations: Available in 2 locations (Hybrid)
Posted Date: October 28, 2025
Work Mode: Hybrid
Work Hours: 12:00 PM – 9:00 PM
About the Role
The Associate Pharmacovigilance Specialist performs pharmacovigilance services such as biomedical literature monitoring, adverse event assessment, indexing, and abstracting. The role requires broad knowledge of scientific terminology, drugs, therapeutic areas, and pharmacovigilance regulations.
You will play a key role in identifying, reviewing, and reporting adverse events from biomedical literature to ensure compliance with global pharmacovigilance standards.
Key Responsibilities
Screen and review biomedical literature to identify potential safety information for pharmaceutical products.
Assess adverse events for regulatory reporting in line with pharmacovigilance regulations.
Conduct regular literature reviews to capture and report relevant safety cases.
Index and abstract scientific data accurately using commercial or client-specific databases.
Maintain compliance with internal SOPs, timelines, and quality standards.
Education and Experience
Qualification: Master’s Degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.)
Experience: Fresher or up to 2 years of experience in reviewing biomedical literature for adverse event reporting
Equivalent combinations of education and experience (e.g., Information Science with ≥1 year relevant experience) are acceptable.
Preferred: Prior experience in Drug Safety / Pharmacovigilance
Skills & Competencies
Strong analytical ability to summarize biomedical case reports, studies, and topics
Working knowledge of biomedical and pharmacological terminology
Familiarity with drugs, therapeutic areas, and PV regulations
Experience with biomedical literature databases (commercial or client-specific)
Excellent written and verbal communication skills
Detail-oriented with strong organizational and time management abilities
Desirable Qualifications
Certification from a Professional Medical Writers Association
Background in scientific or medical writing
Experience using PV literature monitoring tools
Degree in Dentistry, Physiotherapy, or Nursing (with hospital exposure) is an advantage
About the Team
The Pharmacovigilance Team at Clarivate consists of skilled professionals located across India, each reporting to regional team managers. The team combines expertise in market research, consulting, and healthcare analytics, particularly in medical devices and pharmaceutical safety domains.
Work Details
Schedule: 12:00 PM – 9:00 PM (Regular working hours)
Work Mode: Hybrid
Equal Employment Opportunity Statement
Clarivate is an Equal Opportunity Employer, ensuring fair treatment in hiring, compensation, promotion, training, and employment conditions.
All qualified applicants will receive consideration without discrimination based on:
Race, color, religion, gender, sexual orientation, gender identity, national origin, disability, or any other protected characteristic.
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