Associate Pharmacovigilance Specialist

Roles & Responsibilities
• Critically analyze biomedical literature for identification of Individual Case Safety Reports (ICSRs)
• Identify adverse events and other safety-relevant information from published sources
• Perform literature monitoring in line with global regulatory requirements
• Write clear and concise safety narratives summarizing ICSR criteria
• Review drug labels and therapeutic area information for safety assessment
• Ensure timely and accurate drug safety review and reporting
• Maintain audit-ready documentation within drug safety databases
• Adhere strictly to SOPs and pharmacovigilance compliance standards
• Support quality checks and internal review processes
• Contribute to continuous improvement in literature screening workflows

Qualification
• Master’s Degree in Pharmacy, Microbiology, Biotechnology, Biochemistry, Biophysics, Life Sciences, or Biomedical Sciences

Experience
• Fresher or up to 2 years of experience in biomedical literature review for adverse event reporting
• Experience in pharmacovigilance literature screening (preferred)

Skills
• Strong understanding of biomedical and medical terminology
• Knowledge of pharmacovigilance regulations and safety reporting requirements
• Analytical thinking and summarization skills
• Familiarity with literature databases such as PubMed and Embase
• Excellent written and verbal English communication skills
• Strong time management and adherence to SOPs
• High attention to detail and documentation accuracy

About the Organization
Clarivate is a global information services provider supporting innovation across life sciences, healthcare, academia, and intellectual property. Through advanced analytics, scientific data solutions, and regulatory intelligence services, Clarivate helps organizations accelerate research, ensure compliance, and make informed decisions in drug safety and pharmacovigilance operations.