Job Summary
The UCSF Neuroimmunology and Glial Biology Division in the Department of Neurology conducts research trials of investigational drugs, therapies, and on the natural history of multiple sclerosis and other inflammatory and neurodegenerative neurological diseases. We are looking for a highly motivated Clinical Research Coordinator with a strong work ethic, and excellent critical thinking and time management skills. The Clinical Research Coordinator will function as the lead coordinator assigned to new and ongoing studies, including novel first in disease, early stage and investigator-initiated trials, and provides a supportive role as back-up and/or blinded CRC to others in the group assigned other trials.
The Clinical Research Coordinator (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 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.
The CRC\'s duties may include, but will not be limited to supporting the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity; 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, assist with training of Assistant CRCs, 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.
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Organization
Campus
Req Number
74449BR
Employee Class
Career
Percentage
100%
Shift Length
8 Hours
Shift
Days
Additional Shift Details
Monday - Friday 8:30AM - 5PM (some evening and/or weekend may be required)
Bargaining Unit
University Professional Technical Employees - Research Support Professionals Unit (UPTE-RX)
Job Category
Research and Scientific
Required Qualifications
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