Clinical Interface Core (CIC)

The Clinical Interface Core and its Clinical Research Center (CRC) at UIC provides a comfortable, safe and effective environment to conduct research involving human subjects. This is achieved by providing the necessary environment, equipment and personnel to optimize research goals. The CIC fosters education in clinical research at all levels of training.
Read the CI Core full description

NEW On-line Request Form for CCTS Services

Interested in any services from CCTS? We now have an on-line, integrated form. Click the button below to get started.

UICollaboratory Research Profiles

Are you looking for collaborators, mentors, or faculty expertise in a specific subject area? The UICollaboratory can help. Click the button below to explore. For more information, help and FAQs [more]

CIC Application

Application Process

Application Forms

Please follow these steps to complete the forms carefully.

Step 1:

Complete and submit  “Research Participant Advocate: Risk Assessment and Management” form.

Step 2a:
Meet with CIC staff, finalize plan to use CIC services. Once your plan is approved by CIC staff, you can initiate the online CCTS Service Request at:  http://go.uic.edu/CCTS_Request.

Step 2b:
Complete and sign “Appendix G” and submit to CIC leadership for signature.

Step 3:
Submit signed “Appendix G” with your signed RPA report to the IRB with your IRB forms.Please note: a completed and signed "Appendix G" takes the place of the previous memo of CIC approval.

Step 4:
Documentation of IRB approval is required before a study is initiated in the CIC. As soon as IRB approval is provided, a copy of the signed IRB approval letter and stamped consents should be submitted to the CIC.

Radioactive Materials Policy: Please click the icon below to download the CIC's radio active material policy.

If you have any questions, please call or email Lauren Walsh , Investigator Interface Coordinator at 312-413-7316 / laurenw@uic.edu.