Clinical Research Coordinator (2of 2)
About The Position
The Cardiovascular Genetics Center within the Department of Medicine, Division of Cardiology has developed a clinical research infrastructure. The goals are to leverage our considerable case volume of patients referred for genetic testing and inherited cardiovascular disease to create a system that will allow for investigator-initiated research studies, to develop cardiovascular genetics cohort studies, to facilitate contributions to multicenter registries, and to facilitate translational and/or industry-sponsored research on novel therapies. 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, clinical genetic counselors, the Director of Clinical and Translational Cardiovascular Genetics Research, and/or the Principal Investigator (PI), 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. This position will involve interacting with patients with inherited cardiovascular disease and their families, including obtaining informed consent for study participation.
Requirements
- Interacting with patients with inherited cardiovascular disease and their families, including obtaining informed consent for study participation.
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.
- Assist with training of Assistant CRCs if needed.
- 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.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
