The Clinical Trials team is here to support your clinical research, translational research, or clinical trial.

Our clinical trial services include study coordination from start-up to close-out; protocol and case report forms development; contracts and budgets; risk analysis; coverage analysis; regulatory support, including IRB applications; recruitment, pre-screening, and enrollment; informed consent; patient exams and interviews; study visits and case reports; adverse event monitoring; data safety and monitoring board, if needed; investigational product management (randomization, maintenance, storage, dispensation); electronic regulatory binder for storage (and allowing or sponsor remote monitoring); biospecimen processing and shipping; and invoicing and collection.

To further discuss, contact Dr. Amoy Fraser, Manager- Clinical Trials at or 407 COM TRIALS (266 8742).

Helpful Links

University of Central Florida Institutional Review Board

CITI Training (GCP and HSP)

UCF College of Medicine eRegulatory Document Management