PTSD-TBI/ INTRuST Clinical Consortium Coordinating Center

One of the primary responsibilities of the Clinical Consortium-Coordinating Center (CCCC) is to assist the efforts of the Clinical Study Sites by providing scientific, strategic, and administrative leadership and support to help fulfill the Consortium's overarching aims. This includes but is not limited to coordinating the adoption of a Uniform Data Set to standardize measurement of psychological health problems related to deployment, and facilitating the rapid selection, design, and execution of clinical studies within the Consortium.

The Clinical Consortium-Coordinating Center (CCCC) is organized to include an Administrative Core and a Data Core. The primary responsibilities of the Administrative Core are Fiscal and Trial Operations. The responsibility for Trial Design and Portfolio Development are shared with the Data Core. The primary responsibilities of the Data Core are Biostatistics and Informatics.

Murray B. Stein, M.D., M.P.H., Director & Principal Investigator of CCCC
Ariel J. Lang, Ph.D., M.P.H., Deputy Director of CCCC
Administrative Core
Nuzhat Beg, M.D., Clinical Trials Research Associate
Shadha Cissell, M.S.W., Liaison to the Data & Safety Monitoring Board
Lisa Kallenberg, M.D., Clinical Trialist, Publications Coordinator
Larry Marshall, M.D., Traumatic Brain Injury Expert
Scott Matthews, M.D., Medical Monitor
James Payumo, M.D., Senior Clinical Research Monitor
Toni Robinson, M.A., Senior Research Coordinator
Farah Shaikh, M.D., Dr. P. H., Clinical Operations Manager
Data Core - Biostatistics
Sonia Jain, Ph.D., Co-Director of Biostatistics
Rema Raman, Ph.D., Co-Director of Biostatistics

Data Core – Informatics
Erik Groessl, Ph.D., Associate Director of Informatics
Steve Talley, Ph.D., Senior Project Manager
Kyle Choi, M.P.H., Community Health Program Representative