UCSF
UCSF
Posted 3 months ago
Full Time
San Francisco, California
In Person
Smart Summary
Responsibilities
The coordinator independently manages and executes clinical research protocols focused on liver disease and transplantation. Responsibilities include overseeing data collection, ensuring regulatory compliance, and coordinating study operations under the direction of the Principal Investigator.
Qualifications
You have experience coordinating clinical research studies, preferably in gastroenterology or a related field. You are proficient in managing research protocols, ensuring regulatory compliance, and overseeing data collection and management for multiple studies simultaneously. A strong understanding of UCSF policies and regulatory requirements is essential for success in this role.
Must Have Skills for ATS
clinical research protocols
data collection
data management
database management
regulatory compliance
human research protection
Job Description
The GI Division Clinical Research Coordinator will support clinical research studies centered on liver disease and liver transplantation. This position functions at a fully proficient, journey-level capacity, with responsibility for independently managing, executing, and coordinating research protocols under the direction of the Principal Investigator (PI). The coordinator may also oversee data collection and study operations for multiple simultaneous clinical research projects, ensuring compliance with established protocols, UCSF policies, and regulatory requirements.
Duties may include, management and coordinating the tasks of multiple clinical research studies, 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 PI supervisor 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.
UCSF
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