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, Director of Clinical & Aerospace Health Research 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