Hello Friends, Please send me matching candidates on [email protected] Role: SAS Admin
Location: Woodcliff Lake, NJ Must be able to do face to face interview. Overview: To support the Biostatistics team by supporting the computing environment. As a senior member of the team, contributing to the overall efficiency and best practice running of the Biostatistics systems, demonstrating the ability to work efficiently and to a high standard within a clinical team environment. Maintenance of Biostatistics data servers including access control, study directory creation and data transferring. Work with external vendors in order to develop or monitor the content and structure of SAS and related Software installations. The contractor’s primary responsibility will be supporting the statistical technical aspects of our computing environment. SAS Applications Server Data access control Global Analysis Environment. Develop and maintain SOPs, SWPs and other related technical documents, providing input and feedback. Provide input in gathering and analysis for business requirements, by CouponDropDown" href="http://www3.jobdiva.com/employers/myjobs/vieweditjobform.jsp?jobid=842962&time=1350586367946&idxstr=00000003542012082215220000842962&lstjobs=1&recc=1"; target=_blank>validation plans, and other related documents and determining and researching SAS software upgrades and related system maintenance issues. Write and Execute systems and macro testing (IQ/OQ/UAT). Requirements: • Bachelor’s degree in Statistics, Computer Science, Mathematics, or a related science discipline. Master’s degree preferred • 5 years experience in a Regulated environment. Pharma industry preferred. • Experience in administration of UNIX and Windows SAS servers in a pharmaceutical/CRO environment. • Some SAS programming experience in a Regulated environment. • Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. • Proven experience with Unix and Windows operating systems. • Programming / Scripting Experience with Perl and Shell. • Understanding Validation and Systems Development Life Cycle • Extensive knowledge of applicable Regulatory (FDA and EU) requirements for the implementation and usage of Computerized Systems in a Research and Development environment. • Hands-on experience with industry tools including biostatistics platforms, ETL, standard reporting and visualization tools (e.g. Base SAS, SAS CDI, SAS Data Miner, JMP, SAS DD, Oracle HLS, Oracle CDC/Waban, Informatica, Business Objects, i/J Review, Spotfire,) a plus. Thanks, Samir [email protected] Rider Consulting Inc. -- You received this message because you are subscribed to the Google Groups "US_IT.Groups" group. To post to this group, send email to [email protected]. To unsubscribe from this group, send email to [email protected]. For more options, visit this group at http://groups.google.com/group/us_itgroups?hl=en.
