June 9, 2022
Full Time
Req Number: 
As a key member of the HIV Research Program and the Global Brain Health Institute, both within the Memory and Aging Center, the Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level to execute, track, and coordinate research protocols. As directed by the Research Manager the incumbent may coordinate the data collection and operations of several concurrent clinical research studies adhering to the research protocols and UCSF and regulating agency policies.

The CRC’s duties may include, but will not be limited to coordinating the tasks of multiple clinical research studies; acting as an intermediary between services and departments while overseeing data and specimen management; managing and reporting study results; creating, cleaning, updating, and managing databases and comprehensive datasets and reports; coordinating staff work schedules, assisting with training of Assistant CRCs; managing submissions to the Institutional Review Board; participating in the review and writing of protocols to ensure institutional review board approval within University compliance; helping to assure compliance with all relevant regulatory agencies; overseeing study data integrity; implementing and maintaining periodic quality control procedures; interfacing with departments to obtain UCSF approval prior to study initiation; maintaining all regulatory documents; reporting study progress to investigators; participating in any internal and external audits or reviews of study protocols; and performing other duties as assigned.