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Biostatistics, Health Services, Epidemiology, or comparable field • Experience in statistical analysis • Experience with R, SAS, STATA, or other coding language • At least one year of experience with secondary
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all appropriate elements of informed consent. Translate complicated research protocol requirements into language easily understandable by research participants and laypersons. • Assist in
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trial consent forms in accordance with GCP and FDA guidelines, ensuring all appropriate elements of informed consent. Translate complicated research protocol requirements into language easily
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