Professional with 1 year of experience at IQVIA, specializing in documentation of over 7,000 Adverse Drug Reactions (ADRs) in Individual Case Safety Reports (ICSRs). Expertise in end-to-end case processing, including data entry, MedDRA coding, and narrative writing using Argus Safety Database. Achieved FDA/EMA compliance and contributed to a 15% reduction in case processing time through effective collaboration.