Job Title: Associate Pharmacovigilance Specialist
Location: Noida, Uttar Pradesh, India
Work Mode: Hybrid
Job ID: JREQ134096
Industry: Life Sciences & Healthcare
Experience Required: Fresher to 2 Years
Associate Pharmacovigilance Specialist – Biomedical Literature Review & Drug Safety | Noida (Hybrid)
Clarivate is hiring an Associate Pharmacovigilance Specialist for its Pharmacovigilance team in Noida, Uttar Pradesh. This hybrid opportunity is ideal for life sciences postgraduates and early-career drug safety professionals seeking hands-on experience in biomedical literature monitoring, ICSR identification, and regulatory-compliant pharmacovigilance operations.
This role focuses on literature-based pharmacovigilance, adverse event detection, indexing, abstracting, and safety data analysis aligned with global regulatory requirements.
Role Overview: Pharmacovigilance & Biomedical Literature Monitoring
The Associate Pharmacovigilance Specialist will be responsible for reviewing large volumes of biomedical literature and internal safety alerts to identify Individual Case Safety Reports (ICSRs) and other safety-relevant information impacting the risk-benefit profile of pharmaceutical products.
The position requires strong analytical skills, knowledge of medical terminology, understanding of therapeutic areas, and familiarity with global pharmacovigilance regulations.
Key Responsibilities
Critically analyze biomedical published literature and internal safety alerts to identify ICSRs
Assess adverse event data in compliance with applicable global regulatory requirements and SOPs
Prepare concise safety narratives summarizing ICSR criteria and relevant safety findings
Evaluate literature in alignment with client drug labels and product safety profiles
Complete literature review batches accurately within defined quality and timeline standards
Document safety assessments in drug safety systems to maintain audit-ready records
Ensure adherence to pharmacovigilance processes and compliance standards
Educational Qualifications
Master’s Degree in Life Sciences, Health Sciences, or Biomedical Sciences
(Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, or related disciplines)
Experience Requirements
Freshers or up to 2 years of experience in biomedical literature review for adverse event reporting
OR
Equivalent combination of education and experience (e.g., Information Science degree with at least 1 year of relevant drug safety support experience)
Technical Skills & Competencies
Strong analytical ability to evaluate and summarize biomedical case reports and research articles
Working knowledge of biomedical terminology, pharmaceutical products, and therapeutic areas
Experience with commercial or client-specific biomedical literature databases preferred
Understanding of global pharmacovigilance regulations and ICSR identification
Preferred Soft Skills
Excellent written and verbal communication skills in English
Strong time management and ability to meet deadlines
High attention to detail and accuracy
Ability to thrive in a fast-paced, process-driven environment
Strict adherence to SOPs and compliance policies
About the Pharmacovigilance Team
The Pharmacovigilance team at Clarivate supports multiple global clients across diverse therapeutic areas. The team offers structured training, a collaborative work culture, and opportunities to gain exposure to different aspects of drug safety operations and customer engagement.
Work Schedule
Location: Noida or Bangalore, India
Hybrid work model
Working Hours:
9:00 AM to 6:00 PM IST
OR
11:00 AM to 8:00 PM IST
Monday to Friday
Equal Employment Opportunity
Clarivate is committed to providing equal employment opportunities in hiring, compensation, promotion, and training. The organization complies with all applicable non-discrimination laws and regulations across its operational locations.
Apply now on ThePharmaDaily.com to build your career in pharmacovigilance, biomedical literature review, and global drug safety operations.
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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Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Frank Scottile Blvd |Missouri :
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China | Quarry Bay |Liaoning :
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Shanghai Shi |Hubei :
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Netherlands |Remote Australia :
Arkansas | Remote Australia |New South Wales :
Ballina | Sydney |Republic of Western Australia :
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Queensland |Melbourne :
South Yarra |United Kingdom :
England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Sheffield |Oxfordshire :
Witney |Ontario :
Renfrew | Uxbridge | Australia | Richmond Hill | Mississauga | North York |Canada :
Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
Heist op den Berg |Flemish Brabant :
Zaventem |South America :
Argentina | Peru |Brazil :
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Koropi | Athens |Greece :
Greece |North Island :
Auckland |New Zealand :
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Austria |Vienna :
Vienna |Catalonia :
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Madrid |Cebu Province :
Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
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Tallinn |Hà Nội :
Hanoi | Hà Nội |Ho Chi Minh :
Ho Chi Minh City |Italy :
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Riyadh | King Abdullah Economic City | Khulais | Jeddah | Rabigh | Najran |Kuala Lumpur :
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Kyiv |Lima Region :
Lima |France :
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South Africa | Midrand |Nišava District :
Niš |Bohemia :
Prague |Chile :
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