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Description & Requirements
Description & Requirements
The Cardiovascular Research Institute at UCSF is seeking a clinical research coordinator (CRC) for observational studies and clinical trials taking place in the intensive care and transitional care units at at UCSF Moffitt-Long Hospital. The CRC will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Principal Investigators (PI).
The CRC will be responsible for the coordination of one or more single or multi-site, active or follow-up observational clinical studies focused on the acute respiratory distress syndrome (ARDS), pneumonia, sepsis, and COVID-19. The incumbent will spend the majority of their time screening for, recruiting, and enrolling patients into clinical studies spanning inpatient hospitalization and long-term follow-up visits (up to one-year post hospital discharge). In addition, the CRC will be responsible for processing blood collected by others (no phlebotomy required), urine, stool, lung fluid, and nasal swabs for enrolled participants. The CRC will be responsible for organizing biological samples for enrolled participants, conducting standardized in-person assessments at follow-up visits, and clinical data collection and data entry in REDCap. The CRC will also help screen patients for ongoing Phase II and III clinical trials; however, this incumbent will not be expected to independently consent or enroll these patients into the trials without a PI present.
In addition, the CRC will help prepare protocols for study initiation; design flow sheets, data forms and source documents; gather and interpret medical, surgical and laboratory data regarding clinical trial participants; apply understanding of inclusion/exclusion eligibility criteria for protocols; record protocol specific treatments and assure collection and shipment of samples; have primary responsibility of keeping participants on study schedules; complete study forms to submit to sponsors and/or appropriate agencies; assist with preparation of reports and tables; participate in any internal and external audits and/or study monitoring visits; attend team meetings; and perform other duties as assigned.
There will be work needed on Saturdays about 33% of the time in exchange for less time during the regular work week of Monday through Friday.