Develop & review CRF/ e-CRF design and create / review of CRF Completion Guidelines/Mock CRF’s.
Create or Review Data Management Plan components, i.e. study summary/data flow diagrams, timelines, critical variables list, etc.
Represent department on clinical trial team, project management and status reporting
Perform, assist and/or coordinate the tasks that are directly related to data management start-up activities, including development of the Data Flow Diagram, review of Data Validation Specifications, defining editing ground rules, CDMS user acceptance testing, etc.
