SAS Developer

We are seeking experienced Senior Statistical Programmers to join our growing Clinical Research team. In this role, you will provide programming expertise across diverse projects, collaborate with cross-functional teams, and play a key part in delivering high-quality data to support regulatory submissions and clinical development. Tasks: Lead statistical programming activities and ensure high-quality deliverables. Develop, program, and validate SDTM and ADaM datasets following CDISC standards. Conduct Pinnacle 21 validation checks and resolve compliance issues. Create and QC define.xml files and related documentation. Review and ensure quality of tables, listings, and figures (TLFs). Support regulatory submissions (FDA, EMA, Health Canada). Mentor and provide guidance to programming team members. Qualification: Min 6 years of experience in clinical trial statistical programming. Proficiency in SAS and strong knowledge of CDISC standards (SDTM, ADaM). Experience with regulatory submissions strongly preferred. Strong project leadership, problem-solving, and communication skills. Master’s or Ph.D. in Statistics, Biostatistics, Epidemiology, Mathematics, or related field. Benefits & Perks: Fully remote flexibility across Canada (with on-site option in GTA). Competitive salary, annual performance bonus, and comprehensive benefits. Generous PTO plus company-wide holiday shutdown at year-end. Opportunity to make an impact in advancing clinical research.

Location: Canada, CA

Posted Date: 11/4/2025