clinicaltranslation.web.cs.illinois.edu

Launch a study with Carle

Rent space at the Biomedical Research Center or access viable tissues collected at Carle Hospital for experiments ranging from advanced biomaterials and drug discovery to gene profiling

Find Illinois researchers

Search contact, publication, and social network information about Illinois faculty to find potential collaborators or mentors

Launch a Study

Designing your study, from research concept and protocol development to gathering pilot data, is a process that is critical to getting your project sponsored.

Develop Research Idea Target Funding Draft Research Protocol Contact Clinical Partner Institution Assess Enrollment Feasibility Negotiate Scope of Work Draft Study Documents Assess Individual Site Feasibility Finalize Protocol and Study Documents SubmitFunding Application

You may need to seek IRB approval from more than one IRB if you are working with a clinical partner: their IRB and the University of Illinois IRB.

Apply for Study Approval from IRB(s) and IBC File with FDA, if applicable Awarded Grant

Clinical study initiation and management is a complicated process and requires a team approach.

Recruit Clinical Research Coordinator Establish Data Management Procedure Revisit Chosen Study Sites Train Site Personnel in Study Procedures Begin Subject Screening Monitor Study Transfer Data to PI

The end of the study or analysis point, including requirements for archiving and sample disposal.

Filing with the IRB (close-out) Collecting All the Pieces Documenting Process Preparing for Record Storage Where to Archive and for How Long?Disseminate Results