Principal 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.

Flexible Working: 50% Hybrid Working

Location:

Uxbridge, UK

It sounds dramatic, but that's exactly what's at stake here.

At Bristol Myers Squibb, we're in the business of discovering, developing, and delivering medicines that genuinely change patients' lives. And behind every successful clinical trial, every regulatory submission, every approved therapy?

There's a team of brilliant statistical programmers making sure the data tells the right story, accurately, compliantly, and on time.

That's where you come in.

You won't be working in a silo either. You'll be embedded in cross-functional teams, partnering with statisticians, data managers, clinical scientists, and external vendors, building relationships across Bristol Myers Squibb's Global Biometrics & Data Sciences (GBDS) organisation and beyond.

You'll be the programming expert that clinical project teams rely on. The person who takes complex, messy clinical data and turns it into clear, submission-ready outputs that regulators trust. You'll design and implement technical solutions that directly influence whether a medicine moves forward, or doesn't.

That means working with CDISC standards, ADaM specifications, SAS programming, and electronic submissions, things you already know inside and out. But it also means something bigger: your technical decisions will have a direct line to patient outcomes.

• Real regulatory impact, You'll lead and support electronic submissions for significant regulatory filings. Your name, your work, your standards will be part of clinical packages that go in front of global health authorities. That's career-defining experience.
• Technical depth + strategic influence, This isn't a heads-down programming role. You'll review statistical analysis plans, shape programming strategy, and advise senior stakeholders on risk and resolution. You'll be in the room where decisions get made.
• The chance to build and shape a team, If you've been waiting for the opportunity to lead, mentor, and develop other technical professionals, this is it. You'll set objectives, coach in real time, and help talented programmers grow, leaving a legacy that outlasts any single project.
• Work that matters at scale, BMS is a global leader in oncology, hematology, immunology, and cardiovascular disease. The trials you support aren't hypothetical, they're actively changing the standard of care for patients around the world.
• A platform to drive change, You'll be empowered to identify inefficiencies, lead improvement initiatives, and influence the future of how statistical programming operates  you have ideas, there's a culture here that wants to hear them.

• Have 7+ years of statistical programming experience in the pharmaceutical or biopharma industry, including hands-on involvement in major regulatory submissions
• Are deeply fluent in SAS, CDISC/SDTM/ADaM standards, and the end-to-end clinical data pipeline
• Understand the full drug development lifecycle, from eDC data collection through to TFLs and e-submission components
• Can hold your own in a room full of statisticians, clinicians, and regulatory experts
• Are proactive about spotting problems before they become crises, and confident enough to communicate them clearly
• Hold a degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences
• Bonus points if you've already led or managed a team of technical professionals, but if you haven't yet, this role is built to get you there.

Because this isn't just a job. It's a chance to apply your most advanced technical skills to a mission that genuinely matters. You'll join a team where your expertise is valued, your voice is heard, and your work has consequences you can actually feel proud of.

We hire people who are serious about their craft, and then we give them the tools, the team, and the trust to do their best work.

#LI-Hybrid

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  .

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