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. Director of Administrative Core
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Administrative Core
Kimberly Aguilar, B.A. Clinical Operations Coordinator Vishal Bansal, M.D. Clinical Trialist Shadha Cissell, M.S.W. Deputy Director of Administrative Core Samantha Hurst, Ph.D., M.A. Liaison to the Consumer Advisory Board Michael Kalichman, Ph.D. Research Ethicist Arthur Kavanaugh, M.D. Conflict of Interest Teresa Marcotte, B.A. Administrative Coordinator Larry Marshall, M.D. TBI Trials Farah Shaikh, M.D., Ph.D. Clinical Trial Monitor James Payumo, M.D. Clinical Trial Monitor Toni Robinson, M.A. Clinical Trials Assistant Jamie Sable, M.D. Medical Monitor Chris Searles, M.D. Medical Monitor Elenor M. Shigley, M.S. Administrative Director Karen Stokes, B.A. Clinical Trial Manager |
Data Core
Sonia Jain, Ph.D. Co-Director Biostats Core Rema Raman, Ph.D. Co-Director Biostats Core Informatics Core Ted Ganiats, M.D. Director of Informatics Core Erik Groessl, Ph.D. Associate Director of Informatics Core |
