Senior Statistical Programmer

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.

What you'll actually be doing

You'll be a key technical voice within ourGlobal 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 managementresponsibilities — 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 SASprograms to generate derived analysis datasets and clinicalTables, 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 likeStatistical 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 projectswith 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

What you bring to the table

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

Education & Background

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

Core Skills & Knowledge

• Strong, proven proficiency in SASfor 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, andSDTM
• Ability to deliver downstream outputsincluding ADaM datasets, Data Definition Tables,and e-submissionpackages
• Confidence with tools like MS Office, XMLand Pinnacle 21
• A solid grasp of regulatory, industry, and technology standards- you understand why the rules exist, not just what they are
• Familiarity with statistical terminology, clinical trial methodology, medical terminology, and protocol designs
• A genuine team player - you communicate well, build bridges across functions, and make the people around you more effective

It'd be a bonus if you also have…

• Deep experience supporting global regulatory filings (NDA, BLA, MAA)within pharma clinical development
• Broad knowledge of the end-to-end drug development processand global regulatory frameworks
• Experience with R orother statistical programming languages
• Familiarity with the Linux operating system

Why this role, why BMS, why now?

Here, your skills aren't just technically valued - they'remission critical. You'll work in an environment that respects your expertise, gives you the autonomy to lead your own work, and connects your daily output to outcomes that genuinely matter.

You'll gain:

• Exposure to the full clinical development lifecycle, from data collection through to regulatory submission
• The chance to work with industry-leading standards and technologiesin a global biometrics function
• A culture that actively encourages you to identify improvements and champion change- your ideas won't gather dust here
• Collaboration with talented, purpose-driven colleagues across global cross-functional teams

#LI-Hybrid

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Bristol Myers Squibb is Disability Confident – Employer

A UK Government scheme

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