<ul><li>Monitor, collect, and evaluate adverse drug reactions (ADRs) and safety data from various sources.</li><li>Ensure timely reporting of adverse events to regulatory authorities in compliance with guidelines.</li><li>Maintain accurate and up-to-date safety databases and patient case records.</li><li>Perform causality assessment, seriousness evaluation, and medical review of reported cases.</li><li>Prepare periodic safety update reports (PSURs) and other regulatory submissions.</li><li>Collaborate with clinical, regulatory, and medical teams to ensure patient safety and compliance.</li><li>Support audits, inspections, and quality assurance activities within the PV department.</li><li>Stay updated on global pharmacovigilance regulations, guidelines, and industry best practices.</li></ul>

Sr. Executive-Pharmacovigilance