This position works under minimal supervision to direct operation of program or project, exercising independent judgment and authority as required. Oversees day-to-day PRMC submission activities, management / support of REDCap PRMS forms, eIRB PRMC queue, facilitate protocol submissions and modifications to ensure timely reviews, approval and activation of new trials. Coordinates PRMC Committee Meetings, performs quality checks, ensure study submission compliance is 100%25 prior to committee review, monitor studies in the parallel-review process, reviews monitoring and query responses, corrective actions, and follows up on outstanding requests. Works closely with the PRMC Chairpersons, CRO, DSMC, COEE and HRPP/IRB personnel to ensure appropriate routing of cancer-related trials, identify trends, process improvements. Prepares PRMC approval documents, monthly PRMC Decision Report, PRMC- IRB Parallel Review Reports and other special reports as assigned. Train and orient employees to PRMS processes including REDCap PRMS forms. Maintain PRMC Files and reporting parallel review activity.
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Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees