Statistical Programmer

Aurora  ‐ Onsite
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Keywords

Description

  • Under moderate guidance, designs, develops, evaluates and modifies SAS programs to analyze and evaluate clinical data.
  • Plans, writes and executes statistical programs designed to analyze data from database. Produces tables, listings and figures. Assesses data accuracy and consistency.
  • Applies extensive knowledge and skills, may act as lead programmer on project team(s). Consults in the design and development of clinical trials, protocols and case report forms.
  • May supervise one or two lower level programmers assigned to project and/or may provide performance feedback in review of others.
  • Validates, documents and archives single-use programs. Validates and documents SAS macro library.
  • Explores new programming technology. Tests, documents and integrates software tools into programming procedures. Documents and reviews work processes/SOPs.
  • Acts as SAS representative. Coordinates licensing with other RMD sites. Tracks necessity of SAS patches. Validates SAS installation and updates.
  • Troubleshoots and resolves difficult problems in creative ways, and takes a new perspective on existing solutions, exploring and implementing new concepts and methodologies. Translates technical knowledge into business strategy.
  • Leads internal/external teams and builds professional relationships.


  • Minimum Work-Related Experience:
  • 5+ years of relevant work experience as a statistical programmer using SAS in pharmaceutical, biotechnology, diagnostics or medical device environment.
  • Start date
    08/2014
    From
    Real Staffing
    Published at
    07.08.2014
    Project ID:
    754333
    Contract type
    Permanent
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