Senior Statistical Programmer / Principal Statistical Programmer

Senior / Principal Statistical Programmer Experience Senior Statistical Programmer: 7+ years Principal Statistical Programmer: 9+ years Role Summary Responsible for end-to-end statistical programming activities for clinical studies, from specification creation through regulatory submissions, ensuring high-quality and compliant deliverables. Key Responsibilities Develop and validate SDTM, ADaM, and TLFs. Create and review programming specifications. Support regulatory submissions and ensure CDISC compliance. Perform QC and maintain programming standards. Collaborate with cross-functional teams and support study deliverables. Contribute to process improvements and mentoring activities. Required Skills Strong SAS programming expertise; R knowledge is a plus. Hands-on experience with SDTM, ADaM, TLFs, and regulatory submissions.

Good understanding of CDISC standards and clinical trial processes. Leadership Requirements Senior Statistical Programmer: Mandatory co-lead study experience. Principal Statistical Programmer: Mandatory lead study experience.