The Cancer Consortium's participation in the National Cancer Institute's (NCI) National Clinical Trials Network (NCTN) is overseen by Clinical Research Support.

CRS supports the Alliance, ECOG-ACRIN, NRG Oncology, and SWOG NCTN groups.

Key Contacts

StudySupport@fredhutch.org if interested in participating in an NCTN trial

Support Model

CRS partners with study teams to manage NCTN trials. The model for managing NCTN trials may vary depending on the capacity of the investigator’s study team and complexity of the study. General examples are included below.

CRS Support Services

  • Study startup and budget
  • Regulatory
  • Eligibility verification and registration 
  • Patient calendars
  • Data management
  • Serious Adverse Events (SAE) reporting
  • Prepare for audits/monitoring visits
  • Interface with sponsor contacts

Study Team Contributions

  • Local PI
  • Patient identification
  • Consent: discussion and documentation
  • Initial eligibility screening
  • Patient visit/procedure coordination