Senior Statistical Programmer

Title: Senior Statistical Programmer
Locations: Uxbridge - GB
Country: United Kingdom
Country code: GB
Time type: Full time

Description:
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.

This is work that transforms the lives of patients, and the careers of those who do it.

Location: Uxbridge, UK
Hybrid Working: 50% Onsite

Are you ready to turn clinical data into life-changing decisions?
At Bristol Myers Squibb , we believe that behind every dataset, every line of code, and every submission package, there's a patient waiting for a better option. As our Senior Statistical Programmer , you are one of the people who makes that happen.

This isn't a role where your work disappears into a black box. Here, your programming expertise directly shapes how new medicines are developed, reviewed by regulators, and ultimately approved for patients around the world. That's a pretty remarkable thing to be part of.

You'll be a key technical voice within our Global Biometrics & Data Sciences (GBDS) function, working closely with cross-functional clinical teams, collaborating with external vendors, and owning your programming workload with real autonomy.

This is a focused individual contributor role - no line management responsibilities — so you can put your energy exactly where it matters most: delivering high-quality, high-impact programming work.

Day to day, that looks like:

• Writing and validating SAS programs to generate derived analysis datasets and clinical Tables, Figures, and Listings (TFLs) - work that feeds directly into regulatory decision-making
• Contributing to electronic submission preparation (think NDA, BLA, MAA ) — real regulatory milestones that mark pivotal moments in a medicine's journey
• Reviewing and shaping key planning documents like Statistical Analysis Plans (SAPs) and Data Presentation Plans , ensuring clarity and completeness before programming work begins - your input genuinely steers project direction
• Partnering with vendors on programming standards, specifications, and file transfers , building the kind of collaborative relationships that make complex programmes run smoothly
• Independently leading programming assignments across multiple projects with minimal supervision - you'll have real ownership and the trust to match it
• Spotting opportunities to improve efficiency and consistency across GBDS, contributing to initiatives that make the whole team better

We're looking for someone with a solid foundation and the drive to apply it meaningfully. Here's what we need:

• A Bachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences
• Demonstrated industry experience in statistical programming

• Strong, proven proficiency in SAS for producing derived analysis datasets and TFLs
• In-depth understanding of clinical data structures , including CDISC standards (SDTM, ADaM) and relational databases
• Hands-on experience with upstream data handling - multiple data forms, eDC , workflow, and SDTM
• Ability to deliver downstream outputs including ADaM datasets, Data Definition Tables, and e-submission packages
• Confidence with tools like MS Office, XML and Pinnacle 21
• A solid grasp of regulatory, industry, and technology standards - you understand why the rules exist, not just what they…