Responsibilities: Manage clinical trial databases: Review synopsis and attend Synopsis Review Committee (SRC) meeting Review protocols for proper data capture including Case Report Form (CRF) design and CRF completion guidelines Design eCRF specifications according to the protocol Develop eCRF guidelines according to design of the eCRF Lead eCRF development until finalization along with Study Team members Assigned to more complex studies Lead in the development of a Data Management Plan (DMP), when applicable, that outlines CRF flow, data queries, manual checks, and data listings needed to facilitate data cleaning in accordance to our Comprehensive Data Review Plan (CDRP) Develop and test edit specifications Develop scripts for UAT as well as perform/coordinate UAT testing
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