Clinical Research Implementation Office (CRIO)

The CRIO team is available to ensure agile, responsive, evidence-based tools and guidance for clinical translational research and clinical trial implementation across the research lifecycle from concept through publication, °®ÎÛ´«Ã½-wide.  

With a combined 30+ years of NIH RO1/UG3-UH3, multi-site CPRIT, DoD and sponsored clinical research experience, our team is here to help principal investigators and study teams across all schools, departments and divisions.

 

CRIO flowchart

 

Services CRIO provides to researchers 

  • Study Start-up Checklists   

  • Study Timeline Templates with milestones 

  • Recruitment & Retention Plans & Guidance  

  • Investigator Initiated Study Protocol Templates 

  • Data Collection Case Report Form (CRFs) Templates & Guidance 

  • Regulatory File guidance and Templates, including Complion e-Regulatory System  

  • °ä±ô¾±²Ô¾±³¦²¹±ô T°ù¾±²¹±ô²õ.²µ´Ç±¹â€¯Registration & Reporting assistance 

  • Team Science, Training, Collaboration & Resources  

  • FDA IND/IDE Registration & Reporting assistance  

  • Study Team °¿²Ô²ú´Ç²¹°ù»å¾±²Ô²µâ€¯Templates & Guidance  

  • Training for Study Start Up Acceleration 

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