University of California San Francisco
Clinical Research Supervisor
University of California San Francisco, San Francisco, California, United States, 94199
The Clinical Research Supervisor 1 independently coordinates and is accountable for the overall administration of the Clinical Research Coordinator Core Team. The responsibilities include supervising and assigning duties to CRCs and Assistant CRCs, serving on the Clinical Nuclear Imaging Research Committee (CNIRC), and coordinating and facilitating monthly meetings. The Clinical Research Supervisor 1 will work with PIs to determine the level of support needed for each study and determine priorities for all team members of the CRC Core. They will monitor the studies the rest of the Core members are working on and ensure that accounts are billed on a monthly basis with the appropriate level of effort that the CRC assigned to the study dedicated for the period.
The Clinical Research Supervisor 1 will also be the subject matter expert in the area of IRB submissions for the department of Radiology. Among the duties, the Clinical Research Supervisor 1 will evaluate research protocols, help with the IRB submission, and monitor its progress as needed.
The Clinical Research Supervisor 1 will monitor the Clinical Research Billing issues for the Department of Radiology. Additional duties will include training new CRCs and Study Coordinators that are inexperienced in IRB or other areas of research, organizing CRC Core meetings, assigning work to the rest of the staff, and taking over research duties from the rest of the staff as needed.
In addition to the former, the incumbent will independently manage multiple research studies including both industry-sponsored clinical trials and investigator-initiated studies. Study management will include CHR/IRB submissions and maintenance, development of informed consent, creation of data collection documents, subject screening and recruitment, informed consent, subject scheduling, and collection of study data. The incumbent will work with study sponsors and facilitate investigator meetings and clinical trial monitoring visits as needed. The incumbent will provide consultation and assistance to other departments regarding study start-up and study logistics. Within Radiology, the incumbent will assist investigators/CRCs with OnCore/ZZ account set-up and APEX research billing review. The incumbent will train new CRCs as needed and oversee CRC Core billing and effort tracking.
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The Clinical Research Supervisor 1 will also be the subject matter expert in the area of IRB submissions for the department of Radiology. Among the duties, the Clinical Research Supervisor 1 will evaluate research protocols, help with the IRB submission, and monitor its progress as needed.
The Clinical Research Supervisor 1 will monitor the Clinical Research Billing issues for the Department of Radiology. Additional duties will include training new CRCs and Study Coordinators that are inexperienced in IRB or other areas of research, organizing CRC Core meetings, assigning work to the rest of the staff, and taking over research duties from the rest of the staff as needed.
In addition to the former, the incumbent will independently manage multiple research studies including both industry-sponsored clinical trials and investigator-initiated studies. Study management will include CHR/IRB submissions and maintenance, development of informed consent, creation of data collection documents, subject screening and recruitment, informed consent, subject scheduling, and collection of study data. The incumbent will work with study sponsors and facilitate investigator meetings and clinical trial monitoring visits as needed. The incumbent will provide consultation and assistance to other departments regarding study start-up and study logistics. Within Radiology, the incumbent will assist investigators/CRCs with OnCore/ZZ account set-up and APEX research billing review. The incumbent will train new CRCs as needed and oversee CRC Core billing and effort tracking.
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