Senior Statistical Programmer


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. As part of the Statistical Programming team, this person will also provide technical expertise to the development of programming standards and procedures.


  • Serve as the primary project team representative, delegating work as appropriate
  • Generate SDTM domains, ADaM datasets, and Define.xml files with proficiency in creating specification files for these domains
  • Generate analysis datasets, tables, figures, and listings to support the analysis of clinical trials data.
  • Review output across programs to ensure consistency
  • Review, maintain, and approve study documents per standard procedures
  • Provide programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests
  • Program, test, and document global utility programs and tools in accordance with standards and validation procedures
  • Provide technical oversight and leadership in the areas of analysis and reporting
  • Participate in the development and/or maintenance of departmental procedures and standards
  • Train and mentor new programmers


  • BS degree in Statistics, Mathematics, or Computer Science or in a related field
  • Minimum of 5 years Biotechnology/Pharmaceutical/CRO industry experience as a clinical trial SAS Programmer programming CDISC data structures
  • Demonstrates extensive knowledge with 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

Apply Online