Study Planning & Protocol Support

healthcare workers and staff in a meeting

Get customized support from clinical research experts who can help plan your study. 

Higher quality

Improve the quality of your clinical research study.

Efficient study start-up

Timely support from study concept to final protocol.

Fewer stipulations

Reduce IRB stipulations.

Plan and pencil
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Research toolkit step icon of a checkmark linked to Determine Study Feasibility
Research toolkit step icon of a participant linked to Recruit Research Participants
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 I can’t say enough about how amazing the service from CTSI has been, and how kind the people have been. They take things that are a mystery to me, and make them very understandable. I would give them five stars every time.

Mark Zmudy
Mark Zmudy, PhD
​​College of Education and Human Service Professions
Read Dr. Zmudy’s story

We’ve very much appreciated our feasibility reviews from CRSC staff. They’ve helped us identify and address potential issues in our study protocols.

Jeff Boissoneault
Jeff Boissoneault, PhD
Department of Anesthesiology
Read Dr. Boissoneault’s story

Every reviewer had expertise in a different area of research, and they each identified potential issues with the protocol and shared concrete recommendations on how it could be improved.

Niloufar Hadidi
Niloufar Hadidi, PhD, APRN, ACNS-BC, FAHA
School of Nursing

Team

Ryan Lee, PhD, MHS
Lead Clinical Research Specialist
612-625-7088
[email protected]

Katherine Ingram, PhD
Clinical Research Specialist
[email protected]

Alissa Jorgenson
Clinical Research Specialist
[email protected]

Ryan Thiel, MA
Clinical Research Specialist
[email protected]

Nicole Tosun, MS, CCRP
Senior Clinical Research Specialist
[email protected]

Allison Wolf, MPH, CPH
Clinical Research Specialist
[email protected]