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Title:Statistical Programmer
Location:NJ - Bridgewater


The Programmer will perform statistical programming to support statistical analysis of the clinical data and submission to regulatory agencies.

  • Generate data listings, tables and figures (TFL) from clinical data, using SAS or other statistical software
  • Create SAS tools to output TFL directly into clinical study reports
  • Review clinical protocols, SAP and case report forms
  • Create SAS tools to extract data from various sources
  • Merge and/or restructure data to create derived analysis datasets, data warehouse, ISS, ISE, CRTS, in support of regulatory submissions
  • Provide programming support to in-house and externally hosted electronic data collection (EDC) systems
  • Provide programming support to produce CDISC compliant databases (e.g. STDM, ODM, ADAM) for regulatory submissions
  • Supervise and mentor less experienced Statistical Programmers

  • B.S. or M.S. in MIS, Statistics, Computer Science, Chemistry or related fields
  • Five years experience in statistical programming for the analysis of clinical data, preferably within biotech/pharma
  • Very good knowledge of SAS programming
  • Good communications and writing skills
  • Ability to collaborate with, and supervise the work, of other programmers

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