Clinical Data Programmer II

The CDP-II is responsible for the design, development, programming, validation, and maintenance of clinical trial databases throughout the study lifecycle. This includes clinical database build, Case Report Form (CRF) design, edit check programming, custom function development, external data integrations, data review listings, and data reconciliation activities. The CDP-II ensures all deliverables comply with company SOPs, ICH-GCP, CDISC standards, and applicable regulatory requirements while supporting high-quality clinical data management.