Motivated M.Pharm (Pharmacology) graduate with foundational knowledge in pharmacovigilance, adverse event reporting, ICSR processing, MedDRA coding, clinical trial phases, ICH guidelines, and Good Clinical Practice (GCP). Experienced in medical literature review, drug safety monitoring, and clinical research documentation. Seeking an entry-level Pharmacovigilance Associate role to contribute to drug safety surveillance, regulatory compliance, and patient safety in the pharmaceutical industry.