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Title:Contract Senior Statistical Programmer
Location:MA - Cambridge

This position will write SAS programs from instructions provided by Biostatisticians and Statistical Programmers to create CDISC data sets, tables, figures, and listings reporting and submitting the results of clinical trials for investigational medications.

  • Experienced with all SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH.
  • Experienced with the CDISC SDTM and ADaM models and transforming raw data into these standards.
  • Experienced with creating all files, documents, and analyses necessary to support an electronic submissions in eCTD format, including ISS/ISE.
  • Experienced working with all types of safety data and coding dictionaries (MedDRA and WHODRL) commonly used by the pharmaceutical industry.
  • Experienced working in a team environment providing technical leadership and solving clinical trial reporting problems of moderate to high complexity within budget and customary time line constraints while assuring high quality standards.
  • Skilled at performing quality control checks of SAS code and output produced by other Statistical Programmers.
  • Knowledgeable regarding software validation and system development life cycle concepts.

  • B.S. in Biostatistics, Statistics, Computer Science, or a related field and a minimum of 3 years of SAS and relevant pharmaceutical industry experience.

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