Sr. Statistical Programmer

  • Contract Duration: 12+ months, REMOTE
  • IT/Technical
  • Boston, MA

Website Lenox Executive Search

Description

12++ month REMOTE Contract role with strong potential to extend over a year. 4+ years Pharma/Biotech industry experience. Rate depends upon experience

Lenox Executive Search is seeking an experienced SAS Programmer to fill an 12+ month contractual role with a global pharmaceutical company. Must have 4+ years statistical programming within the Pharma/Biotech industry.

REQUIREMENTS fothe Sr. Statistical Programmer:

  • B.S./M.S. in Scientific Discipline and 4+ years experience in Biotech, Pharmaceuticals or Clinical Research Organization. Sponsor side Pharma experience required.
  • Codes complex SAS programs (including Macro language, SAS/STAT and SAS/GRAPH) for applications designed to analyze and report complex clinical trial data and for electronic review, exchange, transformation, and submission of data in CDlSC SDTM format; consistently meeting objectives of the study
  • Experience creating CDISC data sets by transforming various raw data sources, including different Electronic Data Capture (EDC) databases and Interactive Web Response Systems (IWRS), tables, figures, and listings reporting and submitting the results of clinical trials for investigational medications
  • Performs quality control checks of SAS code and output produced by other Statistical Programmers
  • Demonstrates proficient knowledge of clinical development and medical data
  • MedDRA and WHODD coding dictionary experience
  • Excellent communication skills

Responsibilities of the Sr. Statistical Programmer:

  • Codes complex SAS programs (including Macro language, SAS/STAT and SAS/GRAPH) for applications designed to analyze and report complex clinical trial data and for electronic review, exchange, transformation, and submission of data in CDlSC SDTM format; consistently meeting objectives of the study
  • Performs quality control checks of SAS code and output produced by other Statistical Programmers
  • Demonstrates proficient knowledge of clinical development and medical data
  • Solves complex clinical trial reporting problems and has a proven technical proficiency in supporting daily operations and ensuring that project tasks are completed accurately and on schedule under minimal supervision
  • Creates CDISC data sets by transforming various raw data sources, including different Electronic Data Capture (EDC) databases and Interactive Web Response Systems (IWRS), tables, figures, and listings reporting and submitting the results of clinical trials for investigational medications
  • Works with all types of coding dictionaries (MedDRA and WHODD) commonly used by the pharmaceutical industry
  • Works in a team environment providing technical leadership and solving clinical trial reporting problems of moderate to high complexity within budget and customary time line constraints while assuring high quality standards
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