Clinical Research Coordinator Cardiology
About The Position
The Department of Medicine, Division of Cardiology has developed a clinical research infrastructure within the Division. The goals are to increase industry-sponsored research, create a system that will assist a physician within the division to operationalize an investigator-initiated study, and to develop a general cardiology cohort study. The purpose of this position is to carry out the needed tasks as a part of ongoing and future clinical and translational research projects in the Division of Cardiology. Under the supervision of the Clinical Research Supervisor, the incumbent will perform duties related to the support and coordination of clinical studies, and may receive training and development to prepare and advance to the next level within the series.
Requirements
- Under the supervision of the Clinical Research Supervisor, the incumbent will perform duties related to the support and coordination of clinical studies, and may receive training and development to prepare and advance to the next level within the series.
Responsibilities
- Support the management of and coordinate the tasks of single or multiple clinical research studies, depending on their size and complexity.
- Act as intermediary between services and departments while overseeing data and specimen management.
- Manage and report on study results.
- Create, update, and manage databases and comprehensive datasets and reports.
- Help to coordinate staff work schedules to ensure proper coverage.
- Assist with training of Assistant CRCs, and assist Clinical Research Supervisor and/or PI with oversight of other research staff.
- Manage PI’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 and 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
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
