The Clinical Research Aide will perform daily clinical research activities in accordance with Human Subjects Protection, Good Clinical Practice regulations, IRB policies and approved protocols administered by the Department of Pathology with partnership with the Center for Clinical Research Management (CCRM). This role may assist with assessing patient records required for specified clinical research protocols to extract data, completes data entry, and scans research records. The aide will perform tests on human samples in the clinical lab for an approved clinical trial or study, and generates reports and reviews to ensure the validity of data supports activities to ensure compliance with all Institutional Review Boards (IRB) and the study sponsor.
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Career Level
Entry Level
Education Level
High school or GED