CLIN RSCH CRD

June 23, 2022
Neurology – MAC
Full Time
Req Number: 
64682BR
The Clinical Research Coordinator will perform tasks with general direction in order to coordinate research protocols, as directed by the Principal Investigator (PI). The CRC will schedule research participants, coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.

The individual’s duties may include, but will not be limited to supporting the management and coordinating the tasks of multiple clinical research studies; act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports; coordinate staff work schedules; manage Investigator’s protocols in the Committee on Human Research online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; assist other collaborating studies with translation services (from English into Spanish) when necessary and possible; and perform other administrative duties as assigned.