CLIN RSCH CRD
About The Position
The Clinical Research Coordinator (CRC) will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI). The CRC may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies. The CRC will assist neurologists and other members of the clinical and research team in the Movement Disorders and Neuromodulation division with the coordination of clinical research studies and clinical care, including drug treatments and observational studies, for patients with Parkinson’s disease and other movement disorders. Duties will include frequent interactions with patients, coordinating and attending complex clinic and study visits, collecting research data and managing databases, collecting/processing/shipping biological specimens, managing research case report forms and supplies, and managing regulatory documents. The CRC will support management and coordinate tasks for single or multiple clinical research studies.
Requirements
- Perform independently or with general direction at the fully operational journey level.
- Coordinate data collection and operations of concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
- Assist neurologists and other members of the clinical and research team in the Movement Disorders and Neuromodulation division.
- Coordinate clinical research studies and clinical care, including drug treatments and observational studies, for patients with Parkinson’s disease and other movement disorders.
- Interact frequently with patients.
- Coordinate and attend complex clinic and study visits.
- Collect research data and manage databases.
- Collect/process/ship biological specimens.
- Manage research case report forms and supplies.
- Manage regulatory documents.
- Support management and coordinate tasks for single or multiple clinical research studies.
- Manage Investigator’s protocols in the Committee on Human Research online system.
- Manage renewals and modifications of protocol applications.
- Manage implementation of new studies.
- Participate in review and writing of protocols to ensure institutional review board approval within University compliance.
- 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.
Responsibilities
- Execute, manage, and coordinate research protocols.
- Coordinate data collection and operations of concurrent clinical research studies.
- Assist neurologists and research team with coordination of clinical research studies and clinical care.
- Coordinate and attend complex clinic and study visits.
- Collect research data and manage databases.
- Collect, process, and ship biological specimens.
- Manage research case report forms and supplies.
- Manage regulatory documents.
- Support management and coordinate tasks for single or 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.
- Assist Clinical Research Supervisor and/or PI with oversight of other research staff.
- Manage Investigator’s protocols in the Committee on Human Research online system, including renewals and modifications of protocol applications and 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.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
Number of Employees
5,001-10,000 employees
