CLIN RSCH CRD
UCSF•San Francisco, CA
•$34 - $55•Onsite
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); 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 coordinate various clinical studies on kidney disease patients.
Requirements
- Execution, management, and coordination of research protocols
- Coordination of data collection and operations of concurrent clinical research studies
- Adherence to research protocols, UCSF, and regulating agency policies
- Proficiency in creating research accounts in Apex
- Ability to link patients to research studies and update their status
- Skill in linking encounters to studies and setting research billing flags
- Capability to create lab orders and medication orders in Apex
- Experience in scanning and uploading study consent forms into patient medical charts
- Ability to review lab results, current medications, radiology studies, and provider progress notes for data collection
- Experience in creating and maintaining data entry accounts in Redcap and OnCore
- Certified phlebotomist (if performing phlebotomy)
Responsibilities
- Enrolling patients in and assisting with execution of industry trials for kidney disease
- Enrollment of patients in biospecimen banking study from kidney disease clinic
- Coordinating various smaller pilot studies in clinic
- Maintaining IRBs
- Scheduling patient visits and procedures
- Maintaining accurate research charts and research study binders
- Performing accurate data collection and data entry
- Performing patient follow-up visits according to specific research study requirements
- Completing consent procedures and questionnaires with subjects
- Participating in research meetings
- Managing Investigator’s protocols in the Committee on Human Research (IRB) online system, as well as renewals and modifications of protocol applications and the implementation of new studies
- Participating in the review and writing of protocols to ensure institutional review board approval within University compliance
- Helping assure compliance with all relevant regulatory agencies
- Overseeing study data integrity
- Implementing and maintaining periodic quality control procedures
- Interfacing with departments to obtain UCSF approval prior to study initiation
- Maintaining all regulatory documents
- Reporting study progress to investigators
- Participating in any internal and external audits or reviews of study protocols
- Creating research accounts in Apex
- Linking patients to the research study and keeping their research status updated
- Linking encounters to the study and setting the research billing flag
- Creating lab orders and medication orders in Apex
- Scanning and uploading study consent forms into the patient’s medical chart
- Reviewing lab results, current medications, radiology studies, and providers’ progress notes for data collection into the research study database
- Creating and maintaining data entry accounts in Redcap and OnCore, the online data entry systems for research
- Performing other duties as assigned
- Assisting with other studies within the Division of Nephrology
- Performing phlebotomy as needed (if certified)
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
