Office of Research & Development

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CSR&D Data Monitoring

The CSR&D Data Monitoring Committee (DMC) monitors CSR&D clinical studies that are approved for funding, include human subjects, and may involve randomization. The CSR&D DMC provides an ongoing independent evaluation of the progress of studies, including participant accrual and retention, adverse events monitoring, and analysis plan. DMC review is separate and distinct from Institutional Review Board (IRB) review and approval. The DMC will not evaluate the scientific merit, methodology, or overall design, and budgetary constraints of an IRB approved protocol under review, except where changes to the protocol may result in a change in safety level or monitoring.


CSR&D DMC Managers

Dan Lippe, MA

Tamara Paine, MA, MS, DBA, CCRP

CSR&D DMC Central Office Contact

Lucindia Shouse, MS, CIP

Questions about the R&D website? Email the Web Team.

Any health information on this website is strictly for informational purposes and is not intended as medical advice. It should not be used to diagnose or treat any condition.