Senior Statistical Programmer / Principal Statistical Programmer

Senior / Principal Statistical Programmer\n\nExperience\n\n- Senior Statistical Programmer: 7+ years\n- Principal Statistical Programmer: 9+ years\n\nRole Summary\n\nResponsible for end-to-end statistical programming activities for clinical studies, from specification creation through regulatory submissions, ensuring high-quality and compliant deliverables.\n\nKey Responsibilities\n\n- Develop and validate SDTM, ADaM, and TLFs.\n- Create and review programming specifications.\n- Support regulatory submissions and ensure CDISC compliance.\n- Perform QC and maintain programming standards.\n- Collaborate with cross-functional teams and support study deliverables.\n- Contribute to process improvements and mentoring activities.\n\nRequired Skills\n\n- Strong SAS programming expertise; R knowledge is a plus.\n- Hands-on experience with SDTM, ADaM, TLFs, and regulatory submissions.\n- Good understanding of CDISC standards and clinical trial processes.\n\nLeadership Requirements\n\n- Senior Statistical Programmer: Mandatory co-lead study experience.\n- Principal Statistical Programmer: Mandatory lead study experience.