• Statistical Programmer 2

    Job Locations - | US-Remote
    Posted Date 1 week ago(5/14/2018 11:48 AM)
  • Overview

    As the Senior Statistical Programmer you will be responsible for the development, quality control and documentation of statistical (SAS) programs in support of department projects.


    • Assist in the planning and execution of SAS programming activities for a single project.
    • Assist in the review and input into project requirements.
    • Develop SAS programs in support of clinical trial activities.
    • Perform quality control in support of clinical trial activities.
    • Maintain documentation as appropriate.
    • Deliver individual programming deliverables of medium to high complexity within a single project.
    • Demonstrate full proficiency in technical/programming skills.
    • Contribute broad knowledge of clinical trial activities.




    • Bachelor's Degree in appropriate discipline
    • 5 years pharmaceutical industry based Biostatistics and Programming experience
    • 5 years pharmaceutical industry based experience programming within SAS
    • Strong graphical expereince preferred
    • Oncology, Neuro Science or Immunology experience required

    PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.



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