"Clinical Research Coordinator"

Details

Posted: 25-Dec-25

Location: San Francisco, California

Type: Full-time

Categories: Staff/Administrative

Internal Number: 87283BR

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 Principal Investigator (PI); will coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols and UCSF and San Francsico VA Health Care System (SFVA) and regulatory agency policies.

The CRC position is for a Gastroenterology Quality Improvement and Patient Safety program. The Clinical Research Coordinator will be based at the SFVA working collaboratively Tonya Kaltenbach, MD in the Division of Gastroenterology as well as across other Divisions at the SFVA. The research projects are focused on improving endoscopy quality and advancing education. The incumbent will work closely with physicians and trainees in the endoscopy unit; perform independently or with general direction from the Principal Investigator to execute and manage several concurrent research protocols; coordinate the data collection and operations of studies under the guidelines of the research protocols and in compliance with regulatory agency policies.

Incumbent'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 management; manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports; manage Investigator's protocols in the Institutional Review Board (IRB) 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 using technical reports, presentations, and emails; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned.

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.

To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html