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The Clinical Research Coordinator position is with the Ash Lab in the Department of Psychiatry & Behavioral Sciences and will focus primarily on organizing the lab's noninvasive brain stimulation research studies in a team environment. Initially, this position will specialize in studies related to the Lab's focused ultrasound program. 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); manage IRB protocols and e 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.
The CRC will support the PI, Clinical Research Supervisor and other laboratory faculty to whom this position provides indirect support, in coordination of clinical research studies involving patients with mental health disorders and healthy controls. Duties will include managing regulatory documents and submissions to institutional review boards and the FDA (IDE submission and management), authoring consent forms, creating and modifying study flowcharts and figures using the Microsoft Office suite, Adobe Illustrator and EndNote, maintaining study databases and laboratory server (transferring, uploading, and downloading data files), developing proficiency in operating and troubleshooting study specific equipment, coordinating complex clinic and study visits, managing research case report forms, collecting study specific data reports, interactions with patients.
The final salary and offer components are subject to additional approvals based on UC policy.
Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.
The salary range for this position is $34.32 - $55.19 (Hourly Rate).
The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and high-quality patient care. It is the only UC campus in the 10-campus system dedicated exclusively to the health sciences.
