The following services are offered to clinical research staff and investigators:
Clinical Trials On-Line• Curate and quality assure protocol data
• Bookmark and load all PDF docs for protocols, consents, SROs
• Post protocol alerts within 1-2 hours of request
• Register your protocols to ClinicalTrials.gov and the NCI Clinical Trials Reporting Program
Data Quality
• Case Report Form (CRF) design
• Quality control of CRF data for in-house treatment and observational studies
• Assistance with external audit data preparation
• Data management preparation for FACT accreditation
Disease Registries
• Data collection for observational disease registries
• Data collection for hematology retrospective protocols
• State mandated abstracting and reporting to the California Cancer Registry
• Federally mandated data collection and reporting for all transplants performed at COH
Multi-center Coordination
• Multi-center coordination and support of both interventional and observational studies sponsored by COH
• Data coordinating center for NCI sponsored trial through California Cancer Consortium-Pittsburg (CCC-P) and other externally peer-reviewed grants