Clinical Research Coordinator Gastroenterology
About The Position
The incumbent's duties may include, but will not be limited to supporting the 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 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.
Requirements
- Management and coordination of clinical research studies
- Data and specimen management
- Database and dataset management and reporting
- Coordination of staff work schedules
- Training of Assistant CRCs
- Oversight of research staff
- Management of Investigator’s protocols in the Committee on Human Research online system
- Handling renewals and modifications of protocol applications
- Implementation of new studies
- Review and writing of protocols for IRB approval
- Ensuring University compliance
- Assuring compliance with regulatory agencies
- Overseeing study data integrity
- Implementing and maintaining quality control procedures
- Interfacing with departments for UCSF approval
- Maintaining regulatory documents
- Reporting study progress to investigators
- Participating in audits and reviews
Responsibilities
- Supporting the management and coordinating the tasks of multiple clinical research studies
- Acting as intermediary between services and departments while overseeing data and specimen management
- Managing and reporting on study results
- Creating, cleaning, updating, and managing databases and comprehensive datasets and reports
- Coordinating staff work schedules
- Assisting with training of Assistant CRCs
- Assisting Clinical Research Supervisor and/or PI with oversight of other research staff
- Managing 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
- Participating in the review and writing of protocols to ensure institutional review board approval within University compliance
- Helping 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
- Performing other duties as assigned
Benefits
- Total compensation information available at https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
