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Research-Based Objectives
- Clinical trial development linked with correlative studies. Design, data collection, and analyses of new protocols developed by CRC investigators will be fully supported
- Develop predictive models, identify, and confirm prognostic factors for clinical endpoints including time to treatment, response to treatment, time to progression, and survival
- Develop systems for data exchange between different databases in order to increase access to available clinical data.
Core-Based Objectives
- Further develop CIMS and patient database(s) to assure complete and accurate clinical and laboratory data
- Provide a clinical trial-specific structure to utilize CIMS for CRC clinical trials
- Provide a platform in which CRC investigators performing laboratory studies interface with Biostatistics Core B to request clinical information for analyses
- Coordinate CRC Clinical Advisory Committee (CAC) activities
- Maintain and coordinate regulatory documentation including IRB correspondence, SAE reports, FDA correspondence and audit results for CRC clinical sites
