At Cognizant Technology Solutions, I process and review ICSRs, triage case intake, assess adverse events, and prepare accurate case narratives in line with pharmacovigilance regulations, SOPs, and client requirements. I maintain a 98% quality score while processing 400–500 ICSRs per month and meeting turnaround-time requirements.
I've also supported clinical trial data research, physician credentialing, and investigator profiling through secondary research, data validation, and structured database management. My pharmacy background and experience with MedDRA coding, Argus Safety Database, literature screening, and regulatory compliance support accurate drug safety operations.
