Investigator-Initiated Trial (IIT) - Intervention

(approx. 8 - 16 weeks from submission to enrollment)

Study Start-Up Checklist and Forms

1. Create Protocol [using Intervention Protocol Template (Option 1) or ITHS Interventional Protocol Template (Option 2)]

  • Statistical consultant is available, if needed

2. Research Requirements

3. Clinical Research Program (CRP) Feasibility - Submit all documents to %20crp@benaroyaresearch.org

***MUST have feasibility approval before proceeding to Step 4***

4. Submit any Sponsor Clinical Trial Contract / Agreement along with Review Request for negotiations at CTA@BenaroyaResearch.org, if applicable

5. All new study applications must be submitted using the eProtocol. Please visit the IRB page for additional guidance.

6. Submit study synopsis to appear on BRI website by contacting us at crp@benaroyaresearch.org

***CRP “Letter to Commence” MUST be received before any study activity can occur***