Clinical Research Coordinator Gastroenterology

UCSF • San Francisco, CA

1d

About The Position

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.

Requirements

• Fully proficient, journey-level capacity
• Independently managing, executing, and coordinating research protocols
• Oversee data collection and study operations for multiple simultaneous clinical research projects
• Ensuring compliance with established protocols, UCSF policies, and regulatory requirements
• 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

Responsibilities

• 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
• Perform other duties as assigned

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed