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.

Questions about central startup services for industry-sponsored oncology clinical trials.

Questions about Research Group (RG) and Scientific Review Committee (SRC) reviews.

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 Florence eBinders, how to get started, request an account or access to view Consortium member credentialing documents.

Questions about industry supported clinical research agreements.   

Assistance with ClinicalTrials.gov registration, results reporting and FDAAA regulations.

Questions about the CRS intake review, Clinical Trials Reporting Program (CTRP) and NCI reporting requirements. 

Questions about the National Clinical Trials Network (NCTN).