Job Title: Associate Pharmacovigilance Specialist
Company: Clarivate
Location: Noida, Uttar Pradesh, India (Hybrid)
Category: Life Sciences & Healthcare
Employment Type: Full-time, Hybrid
Working Hours: 9:00 AM – 6:00 PM IST OR 11:00 AM – 8:00 PM IST (Mon–Fri)
Job ID: JREQ134096
Posted Date: February 16, 2026
Role Overview
The Associate Pharmacovigilance Specialist performs pharmacovigilance services, including monitoring biomedical literature for adverse events, reporting, indexing, and abstracting. The role requires strong knowledge of medical terminology, drugs, therapeutic areas, and pharmacovigilance regulations. This is an early-career position suitable for freshers or candidates with up to 2 years of experience.
Key Responsibilities
Critically analyze large numbers of biomedical literature articles and internal safety alerts to identify Individual Case Safety Reports (ICSRs) and other safety-relevant information.
Write concise narratives summarizing ICSRs and other relevant safety information.
Demonstrate understanding of client drug labels and apply that knowledge in safety assessments.
Complete literature batch reviews thoroughly, accurately, and on time according to client standards.
Track all actions and assessments in the drug safety system, maintaining an audit-ready record.
Adhere strictly to SOPs, client guidelines, and regulatory requirements.
Qualifications & Experience
Educational Requirements:
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 reviewing biomedical literature for adverse event reporting.
Alternatively, an equivalent combination of education and experience (e.g., Information Science degree with 1 year of relevant drug/patient safety experience).
Skills & Competencies
Required:
Strong analytical ability to summarize biomedical case reports and studies.
Working knowledge of biomedical terminology, drugs, and therapeutic areas.
Familiarity with commercial or client-specific biomedical literature databases.
Excellent English written and verbal communication skills.
Strong time management and adherence to SOPs and policies.
Highly motivated, detail-oriented, and able to work in a fast-paced environment.
Preferred:
Experience with pharmacovigilance systems or drug safety software.
Ability to adapt quickly and learn multiple therapeutic areas.
Team & Culture
Part of the Pharmacovigilance team at Clarivate, serving multiple global customers.
Provides a supportive working environment with personalized training.
Opportunities to engage in diverse pharmacovigilance tasks and client interactions.
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | surat | Tarasadi | Vadodara | Vapi |Maharashtra :
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Ambala | Gurugram | Haryana | Hisar | Kurukshetra | Panchkula | Rohtak | Shivalik |Punjab :
amritsar | Bathinda | Bela | Chandigarh | ludhiana | Moga | Mohali | Patiala | Phagwara | Rajpura |Andra Pradesh :
Anakapali | Anantapur | Bhimavaram | Chittoor | Guntur | Gurgaon | Kakinada | Mangalagiri | Nellore | Pydibimavaram | Tirupathi | Vijayawada | Visakhapatnam |Tamil Nadu :
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Baddi | Solan |Rajasthan :
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Delhi | India | New Delhi | PAN-India |Assam :
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Hajipur | Patna |Kerala :
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Siliguri |Illinois :
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Dún Laoghaire |Galway :
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China | Quarry Bay |Liaoning :
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Netherlands |Remote Australia :
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Queensland |Melbourne :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Canada |Quebec :
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Brussels |Antwerp :
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Argentina | Peru |Brazil :
Brazil | Sao paulo |Attica :
Athens | Koropi |Greece :
Greece |North Island :
Auckland |New Zealand :
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Austria |Vienna :
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Madrid |Cebu Province :
Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
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Ho Chi Minh City |Italy :
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Japan | Saitama |Tokyo :
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