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Clinical Research Guidance

The CTSI offers detailed guidance for every step of the clinical research process.


Getting Started with Clinical Research Budgeting in CRMS Participant Management Clinical Research Toolbox 

To request CTSI services and support, please complete the CTSI Service Request Form.

Access the eIRB

The IRB requires that all human subject applications, amendments, and notifications be submitted through the eIRB system. 

Learn more about accessing and using the eIRB.

Clinical Trial Facilitation

The CTSI provides expertise on protocol development, the IRB, and other regulatory concerns at $78 per hour. 

For more information, please contact Selvin Ohene at sohene@wakehealth.edu.