Clinical Research and Clinical Trials

The University of Florida’s faculty and staff participate in numerous Human Subjects Clinical Research projects, which include clinical trials that study investigational drugs, devices, and/or procedures.

The UF Office of Clinical Research (OCR) is responsible for reviewing all UF Human Subjects Research studies that meet criteria for any of the following:

• Research Billing Compliance Review
• Contract Negotiation
• OnCore Entry

The OCR supports UF researchers by providing the following services for UF clinical research studies that fall under its purview:

• Budget development and/or negotiation
• ClinicalTrials.gov facilitation
• Contracting
• Coverage Analysis
• Support and training for UF’s clinical research management system, OnCore
• Quality Assurance Program for OnCore data
• Regulatory Assistance
• Research Billing Compliance review and training
• Industry Sponsor Invoicing & Receivables  

For more information, please see the OCR main website:  https://clinicalresearch.ctsi.ufl.edu/.