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Title:Contract SAS Programmer
Salary:Open
Experience:4+
Location:NJ - Northern

Description:
Provide statistical programming and validation support for analysis datasets, statistical tables, figures, and listings.

Responsibilities:
  • Provide statistical programming support for other internal and external requests, e.g. publications.
  • Provide input to the database and CRF development, and create edit check programs and provide feedback to the DM's.
  • Work with external vendors in order to develop or monitor the content and structure of SAS data sets, when necessary Access and convert data to SAS from ClinTrial.
  • Database management system and PC file formats (e.g. MS Excel, text files).
  • Provide input in developing SOP's, SWPs, and other related technical documents. 
  • Strong experience with STDM, Data specifications, annotate DCF's and define XML experience.

Requirements:
  • Bachelor or Master's degree in Statistics, Computer Science, Mathematics, or a related science discipline.
  • Minimum 4 years experience in SAS Programming for Phase I-IV clinical trials in a pharmaceutical or CRO setting.
  • Required Skills: SAS-Base, MACRO, STAT, GRAPH, CDISC, ACCESS, MS Office products.
  • Proven experience with Unix and Windows operating systems.
  • Understand software development life cycle; understand FDA Guidelines.
  • MUST have strong SDTM experience.

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