Principal Statistical Programmer

Bristol Myers Squibb EU Policy; Uxbridge; Hybrid; GBP 70,000 - 90,000; Full time

Benefits offered by this job

Flexible working

Comprehensive benefits

Hybrid work schedule

Job summary

Bristol Myers Squibb in Uxbridge, UK is seeking a Principal Statistical Programmer to lead end-to-end programming for clinical data planning, analysis, and regulatory submissions. You will shape ADaM datasets, write and validate SAS programs, and ensure submissions meet strict regulatory standards.

You’ll collaborate with biostatisticians, data managers, and clinical scientists, mentoring teams and driving process improvements while contributing to life-saving therapies.

Qualifications

• Bachelor’s degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Science.
• 6+ years of industry programming experience, including involvement in regulatory submissions.
• Deep expertise in SAS programming and CDISC SDTM/ADaM.
• Understand end-to-end drug development from trial design to submission.
• Strong communication across technical and non-technical audiences.

Responsibilities

• Lead end-to-end programming delivery from ADaM specs through to TFLs and e-submission components.
• Develop, validate, and troubleshoot complex SAS programs to meet regulatory standards.
• Review SAPs and data presentation plans; identify risks early and propose solutions.
• Champion process improvements and smarter workflows.
• Mentor and support recruitment of future talent.

Skills

SAS programming

CDISC SDTM/ADaM

Regulatory submissions

Leadership

Communication

Education

Bachelor's degree in Statistics/Biostatistics/Mathematics/CS/Life Science

Job 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.

Flexible Working: 50% Hybrid Working

Location: Uxbridge, UK

What if your code could change a life?

Not metaphorically. Not eventually. But directly, through the data you shape, the analyses you run, and the submissions you help bring to life.

This is your seat at the table

As a Principal Statistical Programmer here at BMS, you won't be buried in a back-office function. You'll be central to how clinical data gets shaped, interpreted, and presented to the regulators who decide whether a new therapy reaches the patients who need it most.

You’ll lead programming strategy on real clinical projects. You’ll build the technical solutions that turn raw clinical trial data into the evidence that matters. And when a regulatory submission lands, you’ll know your fingerprints are on it, in the best possible way.

This is a role where your expertise doesn’t just support the science. It drives it forward.

What Your Days Will Actually Look Like

You’ll be hands‑on and highly visible—leading programming teams, partnering with biostatisticians, data managers, clinical scientists and setting the technical direction for how data flows from collection to submission.

Here’s What You’ll Own

• Lead end‑to‑end programming delivery – from ADaM specifications and analysis datasets through to TFLs and e‑submission components. Your work sets the standard others follow.
• Drive quality and robustness – independently developing, validating, and troubleshooting complex SAS programs to meet regulatory expectations and internal standards, so submissions are watertight.
• Shape the strategy, not just execute it – reviewing statistical analysis plans and data presentation plans, identifying risks early, and bringing solutions to the table before problems escalates.
• Champion process improvement – you’ll have the platform and the voice to identify better ways of working and actually make them happen, whether that’s new technology, smarter workflows, or stronger standards.
• Grow the people around you – through mentoring, coaching, and supporting the recruitment of future talent, you’ll leave a mark on careers, not just deliverables.

Why now?

When you contribute here, you’re not programming in a vacuum. You’re building the evidence base for treatments that could redefine how the world manages some of its most challenging diseases.

What You Bring

You’re not here to learn the basics – you’re here to lead. You’ll thrive in this role if you have:

• A Bachelor’s degree (or higher) in Statistics, Biostatistics, Mathematics, Computer Science, or a Life Science
• 6+ years of industry programming experience, including meaningful involvement in regulatory submissions
• Deep expertise in SAS programming and a strong command of CDISC standards (SDTM, ADaM)
• Solid understanding of the end‑to‑end drug development process — from trial design through to submission
• The ability to communicate with clarity and confidence across technical and non‑technical audiences
• A collaborative, proactive mindset — because the best insights come from working closely with others

What You’ll Gain

• Real impact – your work directly supports the development and approval of therapies that patients are waiting for.
• Visibility and leadership – you’ll be known across cross‑functional teams, not just within your own function.
• Room to grow – BMS invests in its people. Whether that’s technical depth, leadership development, or cross‑functional exposure, your career trajectory here is genuinely yours to shape.
• A culture that cares – from flexible ways of working to a global community of scientists, programmers, and clinicians who are united by a shared purpose.

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 [e-mail]. 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

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/<

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.