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Title:Sr SAS Programmer
Location:MA - Lexington

An experienced Sr. SAS programmer to contribute to the success of the programming team through delivery of high quality and timely deliverables. The programmer will develop and maintain general-purpose and ad hoc SAS programs for the analysis and reporting of clinical and/or post marketing data, perform QC task to ensure accuracy, and participate in functional process and technology initiatives.

  • Provide general SAS programming support to Clinical Research and Development.
  • Work closely with statisticians to generate analysis data sets and create tables, listings and graphs for interim analyses, preliminary reports and Clinical Study Reports for in-house use, publications, and/or regulatory submissions.
  • Perform quality control checks on program code and outputs produced by other team members.
  • Conduct data edit checks to ensure the quality of source data.
  • Enhance existing utility programs and develop new utility macros to standardize data processing and output procedure.
  • Review and provide input on programming related documentation including plans and specifications.
  • Manage programming timelines, schedules, and activities on specific programming tasks.
  • Report to Associate Director of Statistical Programming.

  • Bachelor's degree in life science, statistics, mathematics, computer science, or related field required; Master's degree preferred.
  • 5+ years of SAS programming experience in biotech or pharmaceutical industry.
  • Experience in SAS programming language, macros, and procedures.
  • Working knowledge of ISS/ISE, CDISC standards (SDTM, ADaM).
  • Detail oriented, and strong organizational and communication skills.
  • Ability to work in a team environment.

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