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GENERAL RESPONSIBILITIES:

In Phase II-IV clinical research studies, recruits and enrolls subjects and performs other study activities in accordance with good clinical practices, standard operating procedures, study protocols and contractual specifications.

It has been determined that the position of Clinical Research Coordinator requires the performance of certain duties that place the employee at risk of an occupational exposure. For a list of position specific duties considered to place the Clinical Research Assistant at risk, see Occupational Exposure Determination of the PPSP Policy in the MS&G.

SPECIFIC DUTIES: