Join our team as the Institutional Review Board (IRB) Protocol Coordinator!

The IRB Coordinator will join the Clinical Research Support (CRS) team dedicated to supporting clinical researchers across USC schools. The IRB Protocol Coordinator provides personalized assistance, education/training and support to USC investigators and study personnel who are putting together a protocol and application for submission to the USC IRB. As such, this position will work closely or in conjunction with the USC IRB.

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Join our team as the Clinical Research Coordinator!

The Clinical Research Coordinator will join a team of coordinators, serving clinical researchers across USC schools. This role will have the opportunity to work on studies of varying disease types and provide a range of study-related services, ranging from regulatory document preparation, participant recruitment, data collection, and study monitoring. Assist investigators or other staff with aspects of sponsor initiated and investigator-initiated research studies.

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Join our team as the Nurse Practitioner!

The Nurse Practitioner is responsible for providing complete standard and research-related clinical care for patients, assists investigators and their research teams in conducting clinical research, and participates and support operation management when needed.

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NIH Funding Acknowledgment: Important - All publications resulting from the utilization of SC CTSI resources are required to credit the SC CTSI grant by including the NIH funding acknowledgment and must comply with the NIH Public Access Policy.