Clinical Data Management professional with experience working at Pharmaceutical and Contract Research Organizations (CROs). Proficient at maintaining data quality and integrity by providing vendor oversight, monitoring study enrollment, data collection, query resolution, and data cleaning throughout the clinical trial life cycle. Specializes in EDC trials with experience in study and form design, edit check programming, and UAT implementation. Professional skills:-Data cleaning, discrepancy management, and query resolution-Listing Review, ad hoc reporting-EDC trial and eCRF design/ programming-Edit check specification development and testing-EDC Post-production/ database migrations-Data integration strategy-SAE Reconciliation-External data transfers, reconciliation-Vendor management-eCRF data standards development and implementation (CDISC)-Project specific DM Documentation (DMP, CRF Completion Guidelines, end-user training, edit checks/CRF specs, test scripts)-Oracle/ Phase Forward InForm-InForm Central Designer certified-Medidata Rave-SAS knowledgeable