Clinical Trials Office

The Clinical Trials Office provides study management services to UIC faculty conducting clinical research related to the prevention, diagnosis, or treatment of cancer.

Our services include:

• Management of the entire study start-up process including:
  • Budget development & negotiation
  • Protocol Review Committee (PRC) submission
  • IRB Submission
  • Routing for contract negotiation and UIC hospital approvals
• Clinical research coordination
• Data management
• IRB submissions
• FDA submissions
• Study financial management
• Quality assurance monitoring
• Staff training and education

To start-up a study, contact the CTO Start-Up Specialist at [email protected].