SAS Programmer II

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POST DATE 9/11/2016
END DATE 10/9/2016

Alkermes Waltham, MA

Job Classification
Full Time
Company Ref #
Waltham, MA
Entry Level (0 - 2 years)
Job Type
AJE Ref #


td p span span span Alkermes plc is a fully integrated, global biopharmaceutical company developing innovative medicines for the treatment of central nervous system (CNS) diseases. The company has a diversified commercial product portfolio and a substantial clinical pipeline of product candidates for chronic diseases that include schizophrenia, depression, addiction and multiple sclerosis. Headquartered in Dublin, Ireland, Alkermes plc has an R&D center in Waltham, Massachusetts; a research and manufacturing facility in Athlone, Ireland; and a manufacturing facility in Wilmington, Ohio. For more information, please visit Alkermes’ website at  /span /span /span a href="" style="margin: 0px; padding: 0px; color: rgb(0, 135, 204); text-decoration: none;" span span span span /span /span /span /span /a span span span . /span /span /span /p p strong style="margin: 0px; padding: 0px;" u style="margin: 0px; padding: 0px;" span span span SAS Programmer II: /span /span /span /u /strong /p p span span span Alkermes is in an exciting phase of growth that few biotechnology companies achieve, with our diversified portfolio of commercial products and an exciting late-stage pipeline. We are moving ahead with global capabilities, an established approach to innovation, world-class manufacturing, financial strength, and our experienced and dedicated people. To achieve our goals for continued growth, the new position of SAS Programmer II was created in the Clinical Development team. This person will: /span /span /span /p ul style="margin: 0px 0px 9px 25px; padding-right: 0px; padding-left: 0px; color: rgb(0, 0, 0); font-family: "Helvetica Neue", Helvetica, Arial, sans-serif; font-size: 12px; line-height: normal;" li span span span Implement SAS programming and analytical skills using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS. /span /span /span /li li span span span Design, develop, evaluate, validate and modify computer programs using SAS to analyze clinical data. /span /span /span /li li span span span Produce and deliver standard datasets, program edit checks and produce quality tables, figures and listings in a timely fashion and high quality. /span /span /span /li li span span span Use their thorough knowledge of CDISC theory and implementation guidelines to create and validate CDISC standard datasets with minimal instruction or input from the supervisor. /span /span /span /li li span span span Provide input in the design and development of clinical trial protocols, case report forms and clinical databases. /span /span /span /li li span span span Review eCRFs (Case Report Form) to ensure consistency with protocol and adequacy in collecting data to meet objectives defined in the protocol. /span /span /span /li li span span span Annotate eCRFs and write SDTM programming specifications. /span /span /span /li li span span span Develop ADaM programming specifications in collaboration with biostatisticians and other clinical development colleagues. /span /span /span /li li span span span Work closely with clinical operations, data management and statisticians to generate and validates statistical output - tables/listing/figures. /span /span /span /li li span span span Liaise with vendors as needed to facilitate electronic data transfers and statistical programming. /span /span /span /li /ul