Associate Pharmacovigilance Specialist
Company: Clarivate
Location: Noida, Uttar Pradesh, India
Work Mode: Hybrid
Industry: Life Sciences & Healthcare
Job ID: JREQ134096
Posted Date: 16 February 2026
Job Type: Full-Time
Experience Required: Freshers to 2 Years
Education: Master’s Degree in Life Sciences, Pharmacy, or Biomedical Sciences
About Clarivate
Clarivate is a global leader in providing trusted insights and analytics to accelerate innovation across life sciences, healthcare, academia, and technology industries. Through advanced data intelligence, scientific research solutions, and regulatory insights, Clarivate supports pharmaceutical and biotechnology companies in improving drug safety, regulatory compliance, and healthcare outcomes.
The company’s pharmacovigilance and drug safety services help organizations monitor product safety, detect adverse events, and maintain regulatory compliance across global markets.
Job Overview
Clarivate is seeking an Associate Pharmacovigilance Specialist to join its pharmacovigilance team in Noida. This role focuses on biomedical literature monitoring, drug safety data analysis, and adverse event identification to support global pharmacovigilance operations.
The selected candidate will review biomedical literature sources to identify Individual Case Safety Reports (ICSRs) and other safety-relevant information related to pharmaceutical products. The role requires strong knowledge of biomedical terminology, pharmacovigilance processes, and scientific literature analysis to ensure accurate safety reporting in accordance with global regulatory guidelines.
Key Responsibilities
Monitor and analyze biomedical literature to identify potential adverse events and drug safety information.
Identify and evaluate Individual Case Safety Reports (ICSRs) from published literature and internal safety alerts.
Summarize and document safety-relevant findings through structured narratives based on literature review.
Perform indexing and abstracting of scientific literature using pharmacovigilance and biomedical databases.
Apply knowledge of drug labels, therapeutic areas, and pharmacovigilance regulations during safety assessments.
Ensure accurate documentation and tracking of pharmacovigilance activities using drug safety systems.
Maintain compliance with client guidelines, regulatory requirements, and standard operating procedures (SOPs).
Complete literature review batches within defined quality and timeliness standards.
Required Qualifications and Skills
Master’s Degree in Life Sciences, Biomedical Sciences, Pharmacy, Microbiology, Biotechnology, Biochemistry, or related disciplines.
Fresher candidates or professionals with up to 2 years of experience in biomedical literature review or pharmacovigilance are eligible.
Strong understanding of biomedical terminology, drugs, and therapeutic areas.
Analytical skills to evaluate scientific publications and identify safety-related information.
Familiarity with biomedical literature databases and drug safety systems is preferred.
Ability to interpret case reports, clinical studies, and scientific publications accurately.
Strong documentation and data analysis skills.
Preferred Competencies
Effective time management and ability to work within defined timelines.
Strong written and verbal communication skills in English.
High level of motivation and ability to work in a fast-paced environment.
Strong attention to detail and adherence to regulatory and SOP requirements.
Ability to work independently while collaborating with cross-functional teams.
Work Schedule
The pharmacovigilance team operates from India (Noida or Bangalore) with hybrid working arrangements. Standard working hours include:
9:00 AM to 6:00 PM IST, or
11:00 AM to 8:00 PM IST (Monday to Friday).
About the Pharmacovigilance Team
The Clarivate Pharmacovigilance team supports multiple global pharmaceutical clients across various therapeutic areas. The team provides a collaborative work environment with structured training programs, opportunities to develop pharmacovigilance expertise, and exposure to global drug safety practices.
Equal Employment Opportunity
Clarivate is committed to providing equal employment opportunities to all qualified candidates. Employment decisions are made based on merit, qualifications, and business needs, ensuring compliance with applicable employment laws and non-discrimination regulations.
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
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Brazil | Sao paulo |Attica :
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Madrid |Cebu Province :
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