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About the Role

The Clinical Research Coordinator will join the GI Division and be responsible for coordinating clinical research studies related to liver disease and liver transplantation. This role involves executing, managing, and coordinating research protocols under the guidance of Principal Investigators, and potentially managing data collection and operations for multiple concurrent studies.

Responsibilities

• Manage and coordinate multiple 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 training of Assistant CRCs.
• Assist PI supervisor with oversight of other research staff.
• Manage Investigator’s protocols in the Committee on Human Research 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 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 internal and external audits or reviews of study protocols.
• Perform other duties as assigned.

Requirements

• Must be able to perform independently at a fully operational journey level.
• Must have experience coordinating research protocols.
• Must have experience managing data collection and operations for concurrent clinical research studies.
• Must have experience managing Investigator’s protocols in the Committee on Human Research online system.
• Must have experience with renewals and modifications of protocol applications.
• Must have experience with the implementation of new studies.
• Must have experience in the review and writing of protocols.
• Must have experience assuring compliance with regulatory agencies.
• Must have experience overseeing study data integrity.
• Must have experience implementing and maintaining quality control procedures.
• Must have experience interfacing with departments for study approval.
• Must have experience maintaining regulatory documents.
• Must have experience reporting study progress.
• Must have experience participating in audits or reviews.

Skills

• Clinical research coordination
• Data collection
• Data management
• Specimen management
• Database management
• Report generation
• Staff scheduling
• Staff training
• Protocol management
• Regulatory compliance
• Quality control
• Interdepartmental communication

Location

• UCSF

Work Type

• Full-time

Experience Level

• Journey level

About the Company

• The GI Division at UCSF focuses on research studies related to liver disease and liver transplantation.