Principal Statistical Programmer
Bristol Myers Squibb · Uxbridge, UK
BiometricsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Bristol Myers Squibb seeks a Principal Statistical Programmer to lead programming delivery on clinical trials in the Neuroscience therapy area. This senior role involves directing technical strategy, managing programming teams, and ensuring regulatory-quality data presentation for drug submissions.
What they're looking for
- Bachelor's degree or higher in Statistics, Biostatistics, Mathematics, Computer Science, or Life Science
- 6+ years industry programming experience with regulatory submission involvement
- Advanced SAS programming expertise and strong CDISC standards knowledge (SDTM, ADaM)
- Comprehensive understanding of end-to-end drug development processes
- Clear communication skills across technical and non-technical stakeholders
- Collaborative and proactive approach to cross-functional teamwork
What you'll be doing
- Lead end-to-end programming delivery from ADaM specifications through regulatory submissions
- Independently develop, validate, and troubleshoot complex SAS programs to regulatory standards
- Review statistical and data presentation plans to identify and mitigate risks early
- Drive process improvements and implement better workflows and technical standards
- Mentor and coach team members to develop future statistical programming talent
Privacy & handoff
This role links to Bristol Myers Squibb's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.