Clinical Research Coordinator - Pediatric Oncology/Hematology
About The Position
The Helen Diller Family Comprehensive Cancer Center (HDFCCC) is seeking a Clinical Research Coordinator to join the Pediatric Oncology/Hematology research team. The Clinical Research Coordinator will perform independently to execute, manage, and coordinate research protocols, as directed by the Clinical Research Manager and/or the Principal Investigator (PI), and/or the Associate Director for the Clinical Research Programs. The incumbent will coordinate the operations and data collection of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies. Department Overview: Bay Area to receive the prestigious designation of “comprehensive” from the National Cancer Institute (NCI). The HDFCCC integrates the work of researchers and clinicians dedicated to four fundamental pursuits: laboratory research into the causes of cancer progression; clinical research to translate new knowledge into viable treatments; compassionate, state-of-the-art patient care; and population research that can lead to improvements in prevention, early detection, and quality-of-life for those living with cancer. The twin pillars of precision medicine and precision population health guide research and treatment at HDFCCC.
Requirements
- Perform independently to execute, manage, and coordinate research protocols.
- Coordinate the operations and data collection of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
Responsibilities
- Support the management and coordination of tasks for single or multiple clinical research studies (sponsored, cooperative group, and investigator-initiated studies), depending on their size and complexity.
- Act as an 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.
- 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.
- Assist in maintaining relevant regulatory documents in partnership with the Regulatory department.
- 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
