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?:definition
  • A researcher in a study who oversees multiple aspects of the study, such as concept development, protocol writing, protocol submission for IRB approval, participant recruitment, informed consent, data collection, analysis, interpretation and presentation.
  • Individual who is employed and/or involved in any aspect of conduct of protocol driven research. EXAMPLE(S): administrators, clinical and data managers, clinical research pharmacists, clinical research associates, clinical trials compliance coordinators, clinical trials specialists, laboratory technologists, nurses, research services consultants, study coordinators and others
?:hasCUIAnnotation
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Metadata

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Anon_1   (more)
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