Clinical Research Central Office

What We Do

  • Provide budget feasibility and compliance reviews
  • Assist with research billing compliance questions and concerns
  • Generate and negotiate externally-sponsored research budgets on an as needed basis
  • Provide assistance in development of investigator initiated trials
  • Review and assist with LOI submissions
  • Collect and analyze study activation metrics
  • Provide education and support for sponsor-investigator INDs
  • Provide UWCCC-specific protocol templates (e.g., Interventional, Observational, Translational) by contacting CRCO@uwcarbone.wisc.edu
  • Coordinate clinical research conducted by UW researchers at affiliate sites
  • Perform regulatory oversight of external sites
  • Conduct site initiation visits for external sites
  • Assist with data verification and support for external sites conducting research
  • Support and facilitate study activation reviews with clinical services
  • Coordinate visits and training for external sponsored-research monitors
  • Provide as needed data management and/or regulatory services for research groups

Acknowledging the UWCCC

If you receive funding from the UWCCC Core Grant for published research including the use of UWCCC Shared Resources to generate or analyze data, or conduct clinical trials, please reference Acknowledging UWCCC in Publications, Posters and Presentations.