Clinical Research Support

NCTN Study Support

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

NCTN Groups Supported by CRS

  • Alliance
  • NRG Oncology
  • SWOG

NCTN Study Support

CRS partners with study teams to manage NCTN trials. In general, CRS provides the following support:

  • Regulatory
  • Budget
  • Patient calendars
  • Patient registration & eligibility review
  • Data management
  • Serious Adverse Events (SAE) reporting

The study team typically provides:

  • Local PI
  • Patient identification
  • Patient visit/procedure coordination

The model for managing NCTN trials may vary depending on the capacity of the investigator’s study team and complexity of the study.


If you are interested in participating in an NCTN trial, please email the study information to

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