Job Description: Coordinate and ensure the timely completion of all Data Management activities for assigned projects following appropriate regulatory guidelines, and company and department SOPs. Provide technical and Data Management expertise as a member of a cross-functional project team. Write clinical Data Management Plans and associated documents (i.e., database specifications, data entry guidelines) and drive the project team review and approval process. Facilitate clinical trial eCRF development or other data capture processes. Design and build eCRFs in Medidata Rave including database validation checks. Oversee and/or conduct and document the User Acceptance Testing of data entry screens, database build and edit check programming. Process and manage instrument generated data including edit checks using SAS.
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