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Senior Principal Statistical Programmer - Remote within US or Canada

Laboratory Corporation of America Holdings (Covance)

Durham, North Carolina, United States

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">A Senior Principal Statistical Programmer at Labcorp Drug Development has the opportunity to work on a variety of studies. </span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">What you can expect:</span></p><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Multiple Sponsors</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Multiple therapeutic areas, or opportunity to specialize in early oncology</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Excellent opportunities to progress and further your career</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Varied, fast paced environment</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Act as a Lead Statistical Programmer working with an amazing team</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Home-based in the US or Canada</span></li></ul><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">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.</span></p><h2>Education/Qualifications:</h2><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">BSc, preferably in computing, life science, mathematical or statistical subject.</span></li></ul><h2>Experience:</h2><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">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 </span><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">responsibilities of the job.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Extensive experience as lead statistical programmer on complex studies in clinical research.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Substantial knowledge of all aspects of clinical trials from initial study set-up to study completion.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">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.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Broad knowledge of all CDISC requirements related to SDTM and ADaM, including define.xml, </span><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Reviewer's Guide and submission standards.</span></li></ul><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">#LI-REMOTE</span></p>

Job posted: 2021-11-16

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