Description

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.