Associate Pharmacovigilance Specialist
Company: Clarivate
Location: Noida, Uttar Pradesh, India
Work Mode: Hybrid
Job Category: Life Sciences & Healthcare
Job ID: JREQ134096
Job Type: Full-Time
Experience Required: Fresher to 2 Years of Experience in Pharmacovigilance or Biomedical Literature Review
Education: Master’s Degree in Life Sciences, Health Sciences, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, or related fields)
About Clarivate
Clarivate is a global provider of trusted insights and analytics that accelerate innovation across life sciences, healthcare, academia, and intellectual property sectors. The organization supports pharmaceutical and biotechnology companies with scientific intelligence, pharmacovigilance services, and regulatory insights that help ensure drug safety and compliance.
Clarivate’s pharmacovigilance team works with global pharmaceutical clients to monitor drug safety data, evaluate adverse event information, and maintain high standards of regulatory compliance.
Job Overview
Clarivate is seeking an Associate Pharmacovigilance Specialist to support drug safety monitoring through biomedical literature review and pharmacovigilance analysis. The role involves reviewing scientific publications, identifying potential adverse events, extracting safety information, and generating safety reports in compliance with pharmacovigilance regulations.
The specialist will analyze published biomedical literature to detect Individual Case Safety Reports (ICSRs) and other safety signals that may impact the risk-benefit profile of pharmaceutical products.
Key Responsibilities
Biomedical Literature Monitoring
Review large volumes of biomedical and scientific literature to identify potential safety signals and adverse event information.
Analyze published research articles, case reports, and drug safety alerts to detect Individual Case Safety Reports (ICSRs).
Ensure literature monitoring activities comply with pharmacovigilance regulatory requirements and internal standard operating procedures.
Safety Data Assessment and Analysis
Evaluate biomedical case reports to determine the presence of reportable adverse events associated with pharmaceutical products.
Apply knowledge of medical terminology, drug mechanisms, and therapeutic areas when assessing safety information.
Interpret safety data in the context of product labeling and regulatory safety requirements.
ICSR Identification and Documentation
Prepare concise safety narratives summarizing relevant ICSR criteria identified in biomedical literature.
Extract and document safety-related information that may influence the safety profile or risk-benefit assessment of pharmaceutical products.
Pharmacovigilance System Documentation
Record safety assessments and review outcomes in pharmacovigilance databases and drug safety systems.
Maintain audit-ready documentation and ensure accurate tracking of literature review activities.
Quality and Compliance
Complete literature safety reviews within established timelines while maintaining high quality standards.
Adhere to pharmacovigilance standard operating procedures, regulatory guidelines, and internal quality frameworks.
Required Skills and Competencies
Strong analytical ability to interpret and summarize scientific literature and biomedical case reports.
Working knowledge of medical terminology, drug classes, and therapeutic areas.
Familiarity with biomedical literature databases and pharmacovigilance information sources.
Strong attention to detail and ability to process large volumes of scientific data accurately.
Ability to work independently while maintaining strict compliance with regulatory guidelines.
Preferred Skills
Experience reviewing biomedical literature for adverse event reporting.
Exposure to pharmacovigilance safety databases and drug safety monitoring systems.
Familiarity with global pharmacovigilance regulations and reporting standards.
Professional Skills
Strong written and verbal communication skills in English.
Effective time management and organizational abilities.
Ability to work in fast-paced, deadline-driven environments.
High level of professional integrity and adherence to standard operating procedures.
Work Schedule
Standard work hours: 9:00 AM – 6:00 PM IST or 11:00 AM – 8:00 PM IST
Workdays: Monday to Friday
Work Mode: Hybrid (Office locations in Noida or Bangalore)
About the Pharmacovigilance Team
The Clarivate Pharmacovigilance team supports multiple global pharmaceutical clients across a wide range of therapeutic areas. The team offers a collaborative work environment, structured training programs, and opportunities to gain hands-on experience in different pharmacovigilance processes and drug safety monitoring activities.
Equal Opportunity Employer
Clarivate is committed to providing equal employment opportunities and maintaining a diverse and inclusive workplace. All qualified applicants are considered for employment without discrimination based on race, gender, age, disability, or other protected characteristics.
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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Japan | Saitama |Tokyo :
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