The Division of Clinical Research supports the conduct of clinical research for the University of Kansas Medical Center, including:
- Dedicated support from an assigned Portfolio Manager
- Coordination of study activation processes
- Regulatory guidance and training
- Quality assurance support
Coordination with Division of Clinical Research is required for all clinical trials and other studies required to use the Velos CRIS system, with the exception of studies supported by the KU Cancer Center Clinical Trials Office. All studies funded by industry or not-for-profit sponsors require a contract with the KU Medical Center Research Institute, Inc.
Reach us ClinicalResearch@kumc.edu for questions, resources and more inforamtion. Faculty and staff, visit the Division of Clinical Research on the myKUMC intranet.
Clinical Coordinating Center
Investigator-Initiated Clinical Trials (IITs) are pivotal to advancing science and health care. The Clinical Coordinating Center (CCC) is dedicated to supporting the complexities of IITs from protocol design, document development, regulatory support, Food and Drug Administration (FDA) submission, safety monitoring plan review, monitoring and project and multicenter management.
Reach the Clinical Coordinating Center at Clin-Coord-Ctr@kumc.edu for more inforamtion.
Resources Available for External Sponsors
- KU Health System - Laboratory Test Directory
- KU Medical Center Research Site Development Partnership Plan
- eSRA Form – EHR Epic O2
- EHR Epic O2 eConsenting Certification
- Sponsor Guide - Study Start Up
- Reach out to SiteDevelopment@kumc.edu for site development and feasibility support
Clinical & Translational Science Unit
Access specialized research support unit providing high-quality clinical services, space and expertise to investigators and their study teams across both hospital and community-based locations. Visit the CTSU pages on the Frontiers Clinical & Translational Science Institute website.