Miriam

Francis

1. Improved clinical trial data accuracy from 92% to 98% by implementing automated validation checks and standardized data entry protocols across 15 active studies 2. Reduced data curation cycle time by 35% (from 8 days to 5 days per study) by developing automated ETL workflows within Veeva Vault Clinical, processing over 500 patient records monthly 3. Successfully supported 12 FDA submissions by ensuring 100% data completeness and CDISC compliance, with zero data-related regulatory queries or delays 4. Led data standardization initiative across 3 therapeutic areas (oncology, cardiology, neurology), training 25+ clinical research associates on data collection best practices and reducing data queries by 40%