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Statistical programming for clinical trials is moving towards a multi-language environment where submissions to regulatory agencies may include code written in SAS, R and other languages (e.g. python, STATA, etc). The mission of this working group is to develop the content for a process to certify that statistical programmers have the basic skills to function effectively in a mixed SAS and R clinical trial programming environment.

Topics will include:

  • FDA CDISC Standards
  • Relevant SAS and R data structures
  • The basics of managing SAS and R environments
  • Reporting methods in SAS and R
  • Developing tests to compare the results of SAS and R analyses.

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