Master of Science degree in Statistics, Mathematics, Biotechnology, or a related quantitative field plus one year or Bachelors degree plus 5 progressive years of experience in SAS statistical programming for Phase I, II, or III clinical trials. Must have one year of experience with each of the following 1 ensuring compliance with WSOPs, ICHGCP and 21 CFR Part 11 guidelinesstandards for derived dataset and TLF programming; 2 statistical programming using full range of SAS components and functionality BASE, STAT, SQL, MACRO, DATA step, PROC, Options, Functions; 3 programming utility macros to generate reports, tables and listings for statisticians; and 4 building clinical patient databases compliant with CDISC SDTM ADaM standards. Will accept any suitable combination of education, experience, or training.
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