Must have Masters degree in Statistics, Computer Science, Applied Mathematics, Life Sciences, Engineering or closely related field plus three 3 years experience in statistical programming in a clinical trial environment. Must have experience in designing and developing complex programming algorithms; SAS backgroundtools such as SAS SASBase, SASMACRO, SASGRAPH, worldwide regulatory application submission deliverables and ADaM data models and CDISC standard. Strong knowledge of reporting processes SOPs and software development lifecycle SDCL required. Applicant must possess familiarity with clinical data management concepts, understanding of statistical terminology and concepts and ability to comprehend analysis plans which describe statistical methodology to be programmed. Telecommuting permitted. 40 hours per week MF 900am 500pm. Must have proof of legal authority to work in the United States.
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