Description
The External Data Specialist processes external and local laboratory data throughout the clinical trial lifecycle, performs quality control and data entry, reviews eCRF designs and study protocols, maintains reconciliation and change logs, supports data transfer agreements and study reporting, and collaborates with clinical data management and cross-functional teams. The role requires knowledge of ICH/GCP, 21 CFR Part 11, clinical trial methodology, and clinical data management processes, with a preferred health-related bachelor's degree or equivalent experience.
