Description
The Senior Clinical Data Associate provides data management support for clinical trials from study start-up through post-database lock, including database development and testing, data entry and quality control, CRF specification, edit checks, data review, reporting, medical coding, SAE/AE reconciliation, vendor coordination, SAS program quality control, and training. The role supports the Lead Data Manager, may require travel, and requires at least five years of experience plus a bachelor's degree or related experience.
