Senior Statistical Programmer

Senior Statistical Programming Consultant Responsibilities:

• Develop and validate SDTM and ADaM datasets and produce tables, listings, and figures for individual studies and integrated summaries submitted to global health authorities
• Provide technical input during SAP and TLF specification development
• Own CRF annotation and dataset specification documentation across SDTM and ADaM standards
• Review and provide input on data collection instruments, vendor transfer specifications, edit checks, and related study documents
• Contribute programming support to clinical study reports, regulatory submissions, and ongoing safety reporting
• Conduct ad hoc and exploratory analyses for publications, presentations, and internal data review
• Oversee and collaborate with third-party programming vendors to ensure quality and consistency
• Help develop and maintain departmental SOPs, work instructions, and process standards
• Stay current with SAS developments and evolving industry best practices

• Bachelor’s or Master’s degree in a quantitative or computational field; advanced degree preferred
• 6+ years of statistical programming experience in pharma or biotech
• Strong communicator able to work across functions, manage priorities, and meet deadlines
• Deep SAS proficiency in a GxP-regulated environment
• Solid track record with CDISC-compliant dataset development and full programming/validation cycles