Adverse Experience Reporting Coordinator III Job in West Point, Pennsylvania Us
· Determines, on the basis of standard operating procedures and U.S. FDA regulations, the prompt or periodic classification of each adverse experience contained in the reports received for company marketed and investigational products. · Reviews and processes, according to standard operating procedures all adverse experience information received for domestic and non-domestic sources which involve Merck. KEYWORDS: Clinical, Clinical Trial Manager, Clinical Site Manager, Study Manager, Protocol, Clinical Research Associate, CRA, Biostatistician, Statistician, Data Read more […]
February 9, 2011
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