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 Qualifications: 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 #J-18808-Ljbffr