Clinical Research Coordinator
About The Position
The Clinical Research Coordinator's duties may include, but will not be limited to, coordinating the tasks of multiple clinical research studies within the Department of Emergency Medicine; 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; train research volunteers; coordinate all 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
- Coordinating the tasks of multiple clinical research studies within the Department of Emergency Medicine
- 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
- Train research volunteers
- Coordinate all 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
Responsibilities
- Coordinating the tasks of multiple clinical research studies within the Department of Emergency Medicine
- 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
- Train research volunteers
- Coordinate all 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
Benefits
- Total compensation
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What This Job Offers
Career Level
Mid Level
Education Level
No Education Listed
