Set Up Your Clinical and Translational Research Study

Obtain regulatory approvals, recruit participants, and establish data collection methods and protocols.

Please note: the below listings are focused on Irving Institute services and are not inclusive of ALL research services offered throughout CUIMC. For more research support services, please visit the Office of the Executive Vice President for Research website. 

Consultations to help set up your study 

Compliance with regulatory requirements  

Submit your IRB protocol and address IRB feedback  

Develop your data management plan