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Office of Clinical Research Policy and Regulatory Operations (OCRPRO)

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Mission Statement

OCRPRO's mission is to facilitate the clinical research enterprise by providing protocol development and regulatory, clinical trials management and safety oversight for the NIAID intramural and Division of Clinical Research (DCR) programs.

OCRPRO originated in June 2001. branch staff consists of a branch chief, clinical research oversight managers, and administrative support personnel. A contract with Leidos Biomedical Research, provides staffing for key areas of the support that the branch provides. Each oversight manager is responsible for an area of research support and oversees the contract staff’s work.




Last Updated March 05, 2015