Principal Statistical Programmer (Remote)
Are you a statistical programming leader who thrives on owning complex clinical studies, mentoring talent, and delivering high-impact results?
We’re looking for a Principal Statistical Programmer who can combine hands-on expertise with leadership to drive high-quality statistical deliverables across clinical trials. This is a role for someone who enjoys both rolling up their sleeves and elevating the team around them.
What You’ll Own
- Lead programming efforts across clinical trials, early-phase studies, and publications
- Serve as the go-to expert for statistical programming and study execution
- Own end-to-end delivery for at least one study, ensuring quality and timeliness
- Develop and validate SAS programs for datasets, tables, listings, and figures (TLFs)
- Deliver outputs for clinical study reports, including safety and efficacy analyses
- Ensure data integrity through validation, transformation, and QC processes
- Support data standardization and migration (e.g., CDISC)
- Partner cross-functionally to solve data challenges and meet critical timelines
Leadership & Impact
- Mentor and manage a small team (2–4 programmers)
- Elevate team performance through guidance, quality standards, and best practices
- Contribute to hiring and building a high-performing programming team
What Sets You Up for Success
- 5+ years of SAS programming experience in clinical trials
- Strong understanding of clinical development and regulatory requirements
- Proven experience in oncology (required)
- Expertise in CDISC standards and/or data standardization
- Ability to lead multiple priorities with autonomy and accountability
- Strong communicator who collaborates effectively across global teams
Why This Role Stands Out
This isn’t just another programming role—you’ll own studies, influence outcomes, and shape a team. If you’re someone who wants to move beyond execution into true leadership and impact, this is your opportunity.