Statistical Programmer

SUMMARY

This essential team member will be responsible for supporting the SAS statistical programming efforts for clinical and non-clinical projects and studies, including developing, testing, maintaining, validating, and documenting SAS programs to meet the project’s needs.

SCOPE AND RESPONSIBILITIES:

  • Generate analysis datasets, tables, figures, and listings to support the analysis of clinical trials data
  • Generate SDTM domains, ADaM datasets, and Define.xml files
  • Review output across programs to ensure consistency
  • Assist in creation of table mockups under supervision of statisticians

DESIRED SKILLS & EXPERIENCE

  • BS degree in Statistics, Mathematics, or Computer Science or in a related field
  • Minimum of 2 years Biotechnology/Pharmaceutical/CRO industry experience as a clinical trial SAS Programmer programming CDISC data structures
  • Demonstrates knowledge of industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines
  • Excellent organizational skills, time management, and ability to coordinate workload and meet established deadlines
  • Excellent communication and interpersonal skills to effectively work in a team environment under the direction of a lead programmer and statistician.

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