Detail-oriented and motivated professional transitioning into Clinical Data Management, with over a decade of experience in data organization, database management, and information retrieval. Proficient in clinical trial data processes, database systems, and quality assurance practices. Seeking to leverage analytical skills and hands-on clinical data management training to contribute to successful trial execution and data integrity.
CRF Design and Validation, Created and validated Case Report Forms (CRFs) using Medidata Rave and Oracle Clinical. Data Management Plan Development, Gained hands-on experience drafting DMPs, outlining data collection, validation, and reporting procedures. Quality Assurance Workflow, Designed processes to ensure consistency across multi-site clinical trial data. CDM Activities, Hands-on knowledge of study startup, conduct, and closeout, including eCRF design, data validation, query resolution, and database locking/freezing. SAE Reconciliation, Managed Serious Adverse Events (SAE) reconciliation and external data reconciliation. Database UAT, Conducted User Acceptance Testing to validate database functionality.
English