This position is responsible for providing administrative coordination and regulatory expertise for the department’s clinical research studies. The CRC will work with Principal Investigators (PIs) to facilitate and execute studies on a site level by translating internal and industry protocols, maintaining regulatory approvals, obtaining and protecting informed consent, collecting data and source documentation, as well as coordinating activities and outcomes with department, other university units, and sponsors.
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Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed