Associate Pharmacovigilance Specialist – Biomedical Literature Review
Company: Clarivate
Location: Noida, Uttar Pradesh, India
Work Mode: Hybrid
Department: Life Sciences & Healthcare – Pharmacovigilance
Job ID: JREQ134096
Posted Date: 16 February 2026
About the Organization
Clarivate is a global leader in analytics, data intelligence, and regulatory solutions supporting life sciences, healthcare, and research-driven organizations. Its Pharmacovigilance division delivers comprehensive drug safety services to international pharmaceutical and biotechnology clients across therapeutic areas.
Role Overview
The Associate Pharmacovigilance Specialist is responsible for biomedical literature monitoring, adverse event identification, and Individual Case Safety Report (ICSR) assessment. The role involves reviewing large volumes of scientific publications, identifying safety signals, and ensuring compliance with global pharmacovigilance regulations.
This position is ideal for fresh postgraduates or early-career drug safety professionals seeking hands-on exposure to literature surveillance and safety data management within a global PV environment.
Key Responsibilities
Critically review and analyze biomedical literature and internal safety alerts to identify reportable ICSRs and safety-relevant information.
Assess articles for adverse events impacting the risk-benefit profile of client products in accordance with global regulatory requirements and SOPs.
Prepare concise narratives summarizing ICSR criteria and safety findings from each article.
Demonstrate understanding of client product labels and apply this knowledge during safety evaluation.
Complete literature review batches within defined quality and turnaround time standards.
Use validated drug safety systems to document assessments and maintain audit-ready records.
Ensure compliance with pharmacovigilance regulations and client-specific guidelines.
Educational Qualification
Master’s Degree in Life Sciences, Health Sciences, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, or related fields).
Experience Required
Freshers or professionals with up to 2 years of experience in biomedical literature review for adverse event reporting.
Alternatively, candidates with an Information Science degree and at least 1 year of relevant experience supporting drug and patient safety may apply.
Working knowledge of biomedical terminology, drugs, and therapeutic areas is essential.
Experience with commercial and client-specific biomedical literature databases preferred.
Required Skills & Competencies
Strong analytical ability to summarize biomedical case reports and research studies.
Knowledge of global pharmacovigilance regulations and ICSR criteria.
Attention to detail with high data accuracy standards.
Effective time management and adherence to SOPs and compliance policies.
Excellent English written and verbal communication skills.
Ability to work in a fast-paced, quality-driven environment.
Work Schedule
Hybrid work model based in Noida or Bangalore, India.
Working hours:
9:00 AM to 6:00 PM IST
OR
11:00 AM to 8:00 PM IST (Monday to Friday)
About the Team
The Pharmacovigilance team at Clarivate supports multiple global pharmaceutical clients across diverse therapeutic areas. The team offers structured training, continuous learning opportunities, and exposure to end-to-end drug safety operations.
Equal Opportunity Employer
Clarivate is committed to providing equal employment opportunities in hiring, compensation, promotion, and professional development, in compliance with applicable non-discrimination laws and regulations.
Advance your career in Pharmacovigilance, Drug Safety, and Biomedical Literature Monitoring with a globally recognized life sciences organization.
Discover more Pharmacovigilance and Clinical Research opportunities at ThePharmaDaily.com.
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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Mexico |northeastern :
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Sheffield |Oxfordshire :
Witney |Ontario :
Renfrew | Uxbridge | Australia | Richmond Hill | Mississauga | North York |Canada :
Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
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Zaventem |South America :
Argentina | Peru |Brazil :
Sao paulo | Brazil |Attica :
Koropi | Athens |Greece :
Greece |North Island :
Auckland |New Zealand :
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Austria |Vienna :
Vienna |Catalonia :
Barcelona |Madrid :
Madrid |Cebu Province :
Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
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Tallinn |Hà Nội :
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Italy |Lombardy :
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Sofia |Sweden :
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