Perform case intake of Individual Case Safety Reports ICSRs from various sources patients healthcare professionals literature etc Enter and update safety data accurately in pharmacovigilance databases Conduct initial assessment and triage of reported adverse events Assist in coding medical terms using MedDRA Ensure timely and compliant reporting of safety cases to regulatory authorities Support preparation of safety narratives and case summaries under supervision Review source documents for accuracy and completeness Assist with signal detection and ongoing safety monitoring activities Follow SOPs GVP guidelines and global regulatory requirements Collaborate with cross-functional teams clinical regulatory quality as needed Job Types Full-time Permanent Fresher Pay 304 180 41 - 657 797 04 per year Perks Cell phone reimbursement Food provided Health insurance Paid sick time Provident Fund Work from home Work Location In person