MERCK SHARP DOHME CORP – $83,013.00/Year

Must have an MS in StatisticsBiostatistics; Pharmacy, or a Biological Sciences field and 7 years of SAS programming experience in a clinical trial environment. We will also accept a BS and 9 years of SAS statistical programming experience in a clinical trial environment.br br Experience must include developing analysis and reporting statistical programming deliverables datasets, statistical analyses, report tables, and graphics using Infectious Diseases standards and according to quality, compliance and timeliness requirements; SAS and clinical trial programming including data steps, procedures, SASMACRO, SASGRAPH; using statistical analysis methods and clinical data management concepts; using SAS in the environment of UnixLinux; leading projects, including completing programming tasks independently at a project level, following programwide standards and suggestingdeveloping additional standards, and engaging key stakeholders; working with CDISC standards including SDTM and ADaM as well as their implementations; using CDISC Controlled Terminology; generating eSub packages for worldwide regulatory submissions such as ISS, ISE, Define and eCRT, cSDRG, ADRG and BIMOOSI; using define.xml and Pinnacle 21 to evaluate the compliance in SDTMADaM datasets and accompanying data definition documents; and ensuring process compliance and deliverable quality.br br PLEASE NOTE These requirements are considered normal for the Statisticians occupation. The Statisticians occupation is classified in Job Zone 5; an Educational Training code of a Masters degree; and a corresponding SVP range of 8 and above.