The Clinical Research Office provides the following services to the clinical investigators of the UF Health Cancer Institute:
Protocol and Consent Authoring
Protocol Feasibility Assessments and Budget Development
Regulatory Management
- Submissions to Institutional Review Boards (IRBs)
- Submissions to FDA
- Submissions to study sponsors
Clinical Trial Coordination
- Patient education
- Patient recruitment
- Study visit coordination
- Data management and monitoring
- Clinicartrials.gov management
- Research lab processing
Financial Management
- Budget development and contract negotiations
- Study invoicing and payments for services
- Billing Compliance program management
Management of UF Health Cancer Institute groups and committees
Quality Control and Assurance Activities
- Study monitoring for IITs
- Routine and directed audits
- Education and training
Monitoring and Maintenance of NCI Cooperative Group Activities
- Blood and Marrow Transplant Clinical Trials Network (BMT CTN)
- Children’s Oncology Group (COG)
- Cancer Trials Support Unit (CTSU)
- Experimental Therapeutics Clinical Trials Network (ETCTN)
- NRG Oncology Group (NRG)
Project Management Office
The University of Florida Health Cancer Institute Project Management Office provides a variety of services to support and promote successful investigator initiated trials for Cancer Institute members, from concept development to final result dissemination.
Clinical Research Office Compliance Group
The Clinical Research Office Compliance Group provides ongoing auditing for complex through low-risk clinical trials.
Cancer Control and Population Sciences Navigator Team
The Cancer Control and Population Sciences Navigator team assists investigators with trial activation and data reporting requirements.
