Clinical Research Coordinator - Radiology

We are seeking a highly motivated Clinical Research Coordinator to join the brain imaging groups of Dr. Yan Li and Dr. Janine Lupo at the UCSF Department of Radiology and Biomedical Imaging. The ideal candidate will play a pivotal role in coordinating research brain imaging studies. This position requires a strong background in coordination, preferably with experience working directly with clinical research coordination.

The Clinical Research Coordinator 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 Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.

Incumbent’s duties may include, but will not be limited to supporting the management and coordinating the tasks of multiple clinical research studies, depending on their size and complexity; act as intermediary between services and departments while overseeing data and specimen management; enroll and consent patients into research studies; manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports; coordinate staff work schedules, assist with training of staff/learners, and assist Clinical Research Supervisor and/or PI with oversight of other research staff; 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; and perform other duties as assigned.