Masters degree in Statistics or closely related field. 3 years of experience in each of the following Use of statistical techniques such as power and sample size calculation, hypothesis testing ANCOVA, GLM, multiple comparison tests, parametric and nonparametric; Preparation of statistical section of clinical trial protocols; and Development of Statistical Analysis Plan SAP. 3 years of previous CRO or clinical research or pharmaceutical industry experience. Demonstrated knowledge of statistical software SAS and other newly developed statistical software.br br Experience may be gained concurrently. Demonstrated knowledge equivalent to at least 6 months of work experience or equivalent coursework.

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