Solid knowledge of SAS and familiarity with basic statistics and probability knowledge; Write SAS programs or macros for the data management including edit checks; Follow CDISC-compliance guidelines to write SAS programs to generate SDTM data sets and create SDTM specifications; Follow CDISC-compliance guidelines to write SAS programs to generate ADaM data sets and create ADaM specifications; Write SAS programs or macros for the statistical analysis including tables, figures, and listings; Follow statistical analysis plan to create mock up tables; Application of SAS programs to implement statistical methods and analysis of clinical study data; Have thorough understanding of regulatory guidance and statistical methodology as applied to pharmaceutical development. Requirement: Bachelor’s Degree in CS or EE related and 3 years’ experience in SAS Programming. Job in Sparks, MD.
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