Labcorp Sr Principal Stats Programming in Boston, Massachusetts
A Sr Principal Statistical Programmer at Labcorp Drug Development has the opportunity to work on a variety of studies.
What you can expect:
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.
BSc, preferably in computing, life science, mathematical or statistical subject
Typically 8 years of SAS® 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
Broad knowledge of all CDISC requirements related to SDTM and ADaM, including define.xml,
Reviewer's Guide and submission standards
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