Clinical Research Hub
The Clinical Research Hub (CRH) provides leadership, establishes policies, and offers infrastructure to support and advance clinical research.
About
As the Office of Research’s concierge for clinical trials research, CRH takes pride in its role as the catalyst for effective collaboration.
Acting as a crucial liaison between Principal Investigators (PIs), study teams, and the dynamic partners across UF Medicine involved in clinical trials research, CRH ignites synergy and facilitates seamless interactions. Your vision and expertise combined with CRH’s network and guidance creates the perfect environment for transformative discoveries. CRH also extends support to OnCore, a comprehensive clinical trials management system. Team members leverage OnCore to streamline protocol management, participant tracking, and revenue capture as well as deliver actionable reports and analytics.
At UF Medicine, all NIH-defined clinical trials that use a billing calendar or the Investigational Drug Service (IDS) are required to be supported by CRH.
Don’t hesitate to connect with CRH for any inquiries or to request support!
clinical Trials Support
CRH Budget Assistance Form
Fill this REDCap budget assistance form for budget negotiation or feasibility needs.
CRH Closeout Portal Form
Fill this REDCap form to submit closeout requests for 214 accounts and CTOAs.
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Study Intake and revision
Confirmation of Service (COS)
Submit a COS form to request codes and pricing before intake submission.
OnCore and epic support
OnCore Support Desk
Get help with OnCore access, troubleshooting, training, consults, and Contacts & Staff updates.
OnCore Training & Resources
Complete required training to obtain or update UF OnCore access.
Epic Training & Resources
Complete required training to obtain or update UF Epic research access.
Salesforce Form
Use this Salesforce form to manage requests and communications. Please reach out via this contact form or email at COM-CRH@ufl.edu.
news and events
HubTalk Series
A monthly forum, the HubTalk evaluates and identifies improvements to the clinical trial process.
