Associate Pharmacovigilance Specialist
Organization: Clarivate
Location: Noida, India
Work Mode: Hybrid
Job Category: Life Sciences and Healthcare
Job ID: JREQ134096
Date Posted: February 16, 2026
Job Type: Full-Time
About the Role
Clarivate is seeking an Associate Pharmacovigilance Specialist to support drug safety and patient risk management activities through biomedical literature monitoring and adverse event analysis. The role involves reviewing scientific publications, identifying safety-related information, and contributing to pharmacovigilance operations in compliance with global regulatory standards.
The selected candidate will apply knowledge of medical terminology, therapeutic areas, and pharmacovigilance regulations to assess adverse events and support individual case safety reporting. This position offers an opportunity to work in a global pharmacovigilance environment with exposure to diverse therapeutic domains and drug safety processes.
Key Responsibilities
Monitor and analyze biomedical literature and internal drug safety alerts to identify potential adverse events and safety-related information.
Identify and evaluate Individual Case Safety Reports (ICSRs) impacting product safety and risk-benefit profiles.
Prepare concise narratives summarizing safety findings and ICSR criteria from reviewed literature.
Perform safety assessments using knowledge of drug labels and regulatory requirements.
Review biomedical literature batches accurately and within defined timelines.
Maintain audit-ready documentation and track safety assessments using pharmacovigilance systems.
Ensure compliance with standard operating procedures (SOPs) and global pharmacovigilance guidelines.
Educational Qualifications
Master’s degree in Life Sciences, Health Sciences, or Biomedical Sciences, including Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, or related disciplines.
Equivalent combination of education and relevant experience may be considered.
Experience Required
Freshers or candidates with up to 2 years of experience in biomedical literature review for adverse event reporting or drug safety.
Candidates with an information science degree and at least 1 year of relevant experience supporting drug or patient safety may also apply.
Required Skills and Competencies
Strong analytical ability to review and summarize biomedical case reports, studies, and scientific literature.
Working knowledge of biomedical terminology, pharmacovigilance processes, and therapeutic areas.
Experience using commercial or client-specific biomedical literature databases.
Strong written and verbal communication skills in English.
Effective time management and organizational skills.
Ability to work in a fast-paced environment with strong attention to detail.
Commitment to regulatory compliance and adherence to SOPs.
Work Environment and Team
The pharmacovigilance team at Clarivate supports global clients across multiple therapeutic areas. The organization provides a collaborative work environment, structured training programs, and opportunities to gain expertise in drug safety operations and customer engagement.
Work Schedule
Standard working hours: 9:00 AM to 6:00 PM IST or 11:00 AM to 8:00 PM IST (Monday to Friday).
Hybrid work model with operations based in India (Noida or Bangalore).
Equal Opportunity Statement
Clarivate is committed to providing equal employment opportunities and maintaining a workplace free from discrimination. Employment decisions are based on merit, qualifications, and business needs in accordance with applicable laws and regulations.
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Croatia |Zagreb :
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