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
  • Training and Education

To start-up a study, contact the CTO Start-Up Specialist at

For more information:

CTO Org Chart

CTO Personnel

CTO Standard Operating Procedures (SOPs)