Services
We offer fee-based assistance to investigators who need to convert their existing University of Washington Human Subjects Division paper-based studies to the new UW Zipline application. Learn more about Zipline conversion services.
Protocol Development and Budgeting
We offer assistance with drafting investigator-initiated protocols, providing costs for grant budgeting, developing UW Clinical Research Budget and Billing submissions, and creating standard operating procedures.
FDA, IRB, and Compliance Support
We prepare and provide support for review of your Food and Drug Administration, Institutional Review Board, and other compliance submissions to ensure completeness, adherence to applicable requirements, and inclusion of all required documents.
Project Management
RCC project managers oversee research from project startup to closeout, directing technical, protocol-specific operations for multicenter projects and complex clinical trials.
Database Design
We assist with the creation of custom research databases and electronic forms using REDCap, a free HIPAA-compliant data capture program.
Recruitment and Study Implementation
We provide assistance with recruitment, screening, consenting, and overall conduct of study visits. This includes facilitating focus groups, interviews, questionnaires, lab processing, and more.
Clinical Study Monitoring
We provide independent review of clinical study records to help investigators who are required by the FDA or funding agency to have their studies monitored. This independent review helps ensure compliance with federal, state, and institutional regulations and Good Clinical Practice guidelines.
Research Staff Training
We provide training and development to existing or new study staff to help you develop a strong research team.