Questions about Clinical Research Support services or general information.
Assistance with gaining access to Seattle Children's systems for Consortium study teams.
Requests and questions regarding new CRC and PI orientation, training, and resources.
CRS Central Startup
Questions about central startup services for industry-sponsored oncology clinical trials.
Protocol Review and Monitoring System (PRMS)
Questions about Research Group Review (RGR) and Scientific Review Committee (SRC).
Data and Safety Monitoring
Questions about DSMBs and DSMC.
Questions for Reg. Affairs, including review of FDA submissions and correspondence.
Submission of external monitoring reports for review by the Consortium's Compliance Sub-Committee.
Questions about the National Clinical Trials Network (NCTN).
Questions about Florence eBinders, how to get started, request an account, or access to view Consortium member credentialing documents.
Clinical Research Agreements
Questions about industry supported clinical research agreements.
Assistance with ClinicalTrials.gov registration regulations and results reporting and FDAAA regulations.
Clinical Trials Reporting Program (CTRP) Support
Questions about CTRP and NCI reporting requirements.