Minimum Requirementsbr Education Bachelors, or equivalent in pharmacy or related scientific or technicalbr fieldbr Experience 7 years experience within pharmaceutical industry, or CROs supportingbr statistical analysis of clinical trials programmingbr Alternatebr Education Masters, or equivalent in pharmacy or related scientific or technical fieldbr Experience 5 years experience within pharmaceutical industry, or CROs supportingbr statistical analysis of clinical trials programmingbr Special Requirements H14br 1 5 years experience with all aspects of the SAS programming language used in clinicalbr trials programming;br 2 5 years experience with CDISC SDTM and ADaM, for implementation in clinical trialsbr analysis;br 3 5 years experience with the application of statistical concepts in support ofbr analyses and reporting of clinical trials;br 4 5 years experience with all phases of drug development, including early and latebr phase clinical development and submission;br 5 5 years experience with statistical methods using SAS;br 6 5 years experience with database structures and setup; andbr 7 The candidate should have successfully provided programming expertise at the Projectbr level for at least two global development projects that have been submitted tobr regulatorybr agencies.br Experience can be concurrent.

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