Clinical Research Coordinator
About The Position
Under the supervision of the Clinical Research Supervisor, Clinical Research Coordinators (CRC) support the clinical trial management of investigator-sponsored, pharmaceutical-sponsored, and/or other types of consortium trials programs as assigned/needed. Responsibilities include communicating with the Clinical Research Supervisor to ensure aspects of study initiation of protocols are developed after regulatory and budgetary approval, and report study progress to the appropriate PI. The CRC will support 4-5 research studies that are studies in patients with cancer and benign urologic diseases. This may include active and follow-up studies, depending on the complexity of the patients and procedures. Independently, the CRC maintains protocol files, data collection and subject source records, develops project management documents and electronic data forms for each assigned study. The CRC supports the investigator in research study project management to assure compliance with the Code of Federal Regulations and the ICH Guidance on Good Clinical (Research) Practice as well as UCSF Institutional policies and IRB protocols. The CRC also supports the research team with additional duties as assigned (e.g., obtaining archived biospecimens or data for ongoing studies).
Requirements
- Support of clinical trial management
- Communication with Clinical Research Supervisor
- Development of study initiation protocols
- Reporting study progress
- Support of research studies in patients with cancer and benign urologic diseases
- Maintenance of protocol files
- Data collection and subject source records
- Development of project management documents and electronic data forms
- Assurance of compliance with regulations and policies
Responsibilities
- Support the clinical trial management of investigator-sponsored, pharmaceutical-sponsored, and/or other types of consortium trials programs as assigned/needed.
- Communicate with the Clinical Research Supervisor to ensure aspects of study initiation of protocols are developed after regulatory and budgetary approval.
- Report study progress to the appropriate PI.
- Support 4-5 research studies in patients with cancer and benign urologic diseases, which may include active and follow-up studies.
- Maintain protocol files, data collection and subject source records.
- Develop project management documents and electronic data forms for each assigned study.
- Support the investigator in research study project management to assure compliance with the Code of Federal Regulations and the ICH Guidance on Good Clinical (Research) Practice as well as UCSF Institutional policies and IRB protocols.
- Support the research team with additional duties as assigned (e.g., obtaining archived biospecimens or data for ongoing studies).
Benefits
- Total compensation information available at https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
