The Clinical Trials Office assists investigators, scholars, and staff in the conduct of clinical research by providing education in regulatory and clinical research administration, help with study recruitment, and a vast array of static and interactive resources to guide investigational teams through the myriad of local, state, and federal requirements. By supporting investigators with IRB and FDA applications, research budgeting and billing, and cost analysis, the CTSC facilitates efficient compliant clinical research at UC Davis. Additionally, the group provides investigators with access to a highly trained staff of clinical research coordinators who are experienced and trained in the complex clinical research environment and can help monitor, mentor, and foster quality assurance through all phases of a clinical research protocol.
Clinical Trials Office
Patients and Volunteers
We assist members of the community with finding ways to engage with clinical research opportunities.
Breakthroughs that address the health challenges facing our world are at the core of our mission to discover and share knowledge to advance health. UC Davis conducts more than 1,000 research studies annually, including basic science, translational and clinical trial research - all with the goal of bringing new, effective and safe treatments to patients more quickly.
We provide connections with clinical research expertise on campus and offer partnership management to ensure rapid start up of clinical trials. For more information, email the Clinical Trials Office.
Services We Offer
- Complete Study Management
- Study Start-up
- Clinical Trial Consultation
- Clinical Research Coordinators (CRCs)
- IRB Preparation and Review
- FDA Application (IND/IDE)
- Monitoring and Quality Assurance
- Coverage Analysis