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); may assist with assessing patient records required for specified clinical research protocols to extract data; completes data entry, scans research records; performs tests on human samples in the clinical lab for an approved clinical trial or study; generates reports and reviews to ensure validity of data supports activities to ensure compliance with all Institutional Review Boards (IRB) and the study sponsor.
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Job Type
Part-time
Career Level
Entry Level
Education Level
High school or GED