In my Clinical Data Management project, I configured eCRFs, study visits, and participant records in Castor EDC for a simulated clinical trial. I validated data using edit-check rules and documented missing, invalid, and inconsistent data in a query log.
My biotechnology studies and clinical research training covered clinical trial data analysis, ICH-GCP, CDISC, and SDTM. I also completed a Clinical Trial Analysis & Reporting internship, where I trained in clinical data analysis and basic SAS programming.

