Pharmacy Job at Clarivate | Apply Now for the Associate Pharmacovigilance Specialist Role
Clarivate is hiring an Associate Pharmacovigilance Specialist to support global drug safety through literature screening and safety data evaluation. This Pharmacy Job is ideal for candidates looking to build a strong foundation in pharmacovigilance, scientific analysis, and regulatory compliance—while contributing to better patient safety worldwide.
- Position: Associate Pharmacovigilance Specialist-7
- Location: Noida, Uttar Pradesh, India
- Job ID: JREQ134249
Clarivate Job Responsibilities
- Under supervision, evaluate literature reports for potential cases of adverse events or safety concerns requiring further investigation and escalate case processing and follow-up.
- Extract pertinent safety data from identified literature sources, including adverse events, safety signals, and other relevant information, ensuring accuracy and completeness.
- Enter relevant safety data into pharmacovigilance databases or tracking systems, maintaining clear and organized documentation of literature screening activities and outcomes.
- Stay updated on pharmacovigilance regulations, guidelines, and best practices related to literature screening and pharmacovigilance signal detection and incorporate new knowledge into daily activities.
Minimum Qualifications
- Bachelor’s degree or equivalent in Pharmacy
- 1 Year of Relevant Experience
Clarivate Job Summary
Pharmacovigilance literature screening involves the systematic review of scientific and medical publications to detect adverse drug reactions and ensure drug safety. Professionals in this field critically assess research articles, clinical trial data, and other relevant literature to identify potential safety signals and maintain regulatory compliance.
Why This Role?
This role is a perfect opportunity for anyone looking to begin or advance their career in pharmacovigilance with a global leader in research and analytics. As an Associate Pharmacovigilance Specialist at Clarivate, you’ll work at the heart of drug safety—screening scientific literature, identifying safety signals, and supporting regulatory-compliant reporting. This job offers hands-on experience with real-world safety data, exposure to international PV standards, and continuous learning in a highly specialized domain. If you’re passionate about patient safety, analytical work, and building a strong foundation in PV, this role gives you the right platform to grow, contribute, and make a meaningful impact on global healthcare.
