Training A New Nurse Practitioner Sub I On Clinical Trials

Adding new Sub-I's to a study requires a great deal of careful explanation. Sub-I's are sometimes familiar with academic research and understand the purpose of conducting randomized double-blind, placebo-controlled trials but are not familiar with pharmaceutical research. Once a Sub-I is added to a study, they may do things such as refer patients to the study or follow patients throughout the trial. 

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