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About the Role
The Clinical Research Coordinator (CRC) will execute, manage, and coordinate research protocols under general direction. This role supports the management and coordination of single or multiple clinical research studies, acting as an intermediary between services and departments while overseeing data and specimen management.
Responsibilities
- Execute, manage, and coordinate research protocols.
- Coordinate data collection and operations for clinical research studies.
- Support the management and coordination of clinical research studies.
- Act as an intermediary between services and departments.
- Oversee 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 oversight of other research staff.
- Manage Investigator’s protocols in the Institutional Review Board (IRB) online system.
- Manage renewals and modifications of protocol applications.
- Manage the implementation of new studies.
- Participate in the review and writing of protocols to ensure IRB approval.
- 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 internal and external audits or reviews of study protocols.
Requirements
- Must have the ability to perform independently or with general direction at the fully operational journey level.
Work Type
- Limited appointment
Experience Level
- Journey level