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Labcorp Sr Principal Stats Programming in Boston, Massachusetts

Job Overview:

A Sr Principal Statistical Programmer at Labcorp Drug Development has the opportunity to work on a variety of studies.

What you can expect:

  • Multiple Sponsors

  • Multiple therapeutic areas, or opportunity to specialize in early oncology

  • Excellent opportunities to progress and further your career

  • Varied, fast paced environment

  • Act as a Lead Statistical Programmer working with an amazing team

  • Home-based in the US or Canada

Join our growing team and discover your extraordinary potential by working as a Labcorp Drug Development Senior Principal Statistical Programmer within our statistical programming department. As a Senior Principal Statistical Programmer at Labcorp Drug Development you will assume the role of Lead Statistical Programmer for allocated studies, developing, QCing, and maintaining SAS programs to create SDTM and ADaM datasets and TFLs.

Education/Qualifications:

BSc, preferably in computing, life science, mathematical or statistical subject

Experience:

Typically 8 years of SASĀ® programming experience in the CRO or Pharmaceutical industry, or an

equivalent combination of education and experience to successfully perform the key

responsibilities of the job

Extensive experience as lead statistical programmer on complex studies in clinical research

Substantial knowledge of all aspects of clinical trials from initial study set-up to study completion.

Complete knowledge and understanding of the processes and procedures used within a Statistical

Programming environment and the ability to communicate to programmers and non-programmers

alike.

Broad knowledge of all CDISC requirements related to SDTM and ADaM, including define.xml,

Reviewer's Guide and submission standards

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