Senior Statistical Programmer

July 18, 2025
Application ends: October 18, 2025

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Job Description

As part of the interview process you will be asked to complete a short video screening assessment. We can only consider applications who currently hold full working rights for Australia.What You’ll Do

  • Lead Complex Projects: Own the programming lifecycle for high-impact studies—from database integration to statistical output.
  • Innovate with Purpose: Design and implement advanced macros, tools, and process improvements that elevate programming efficiency.
  • Collaborate Across Teams: Work closely with statisticians, data managers, and clients to deliver seamless, high-quality results.
  • Mentor & Guide: Share your expertise with junior programmers and help shape the future of our programming team.
  • Drive Quality & Compliance: Ensure all deliverables meet regulatory standards and internal quality benchmarks.

What You Bring

  • A degree in Computer Science or a related field (Master’s preferred).
  • 3–5 years of experience in statistical programming within clinical trials.
  • Advanced SAS programming skills (Base SAS, SAS Graph, SAS Macro).
  • Experience with R programming will be considered an asset.
  • Strong understanding of clinical data, statistical principles, and regulatory requirements.
  • Advanced knowledge in CDISC standards (SDTM and ADaM).
  • Excellent communication, leadership, and multitasking abilities.
  • Ability to quickly understand and follow processes and tools.

Why You’ll Love Working Here

  • Impact: Your work supports the development of new therapies and improves patient outcomes worldwide.
  • Innovation: Be part of a team that values creativity, continuous improvement, and cutting-edge technology.
  • Flexibility: Enjoy a remote-friendly culture with flexible hours and global collaboration.
  • Growth: Access to training, mentorship, and career advancement opportunities.

Are you interested in this position?

Apply by clicking on the “Apply Now” button below!

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