A critical member of the Human Research Protection Program (HRPP) Office within the Protocol Activation and HRPP Unit in Clinical Research Administration (CRA) , this position provides operational, technical, administrative leadership and expertise in Institutional Review Board/Privacy Board review committee management and oversight to support the achievement of Center goals for Time to Activation and most importantly to ensure the rights and welfare of MSK's research participants are protected. This position is a leader charged with the operational oversight and management of the IRB/PB, and must ensure full compliance with Institutional, State and Federal regulations (i.e. FDA, Office of Human Research Protections,
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