Principal Statistical Programmer

BMS; Denham; Hybride; GBP 70 000 - 105 000; Plein temps

Avantages offerts par ce poste

Flexible Working: 50% Hybrid

Impactful work

Résumé du poste

Bristol Myers Squibb in the UK is seeking a Principal Statistical Programmer to join our GBDS-focused team. You will turn complex clinical data into submission-ready outputs for regulatory filings, shaping programming strategy and influencing decisions that affect patient outcomes.

You'll work with SAS, CDISC SDTM and ADaM standards, and be embedded in cross-functional teams of statisticians, data managers, and external vendors, delivering end-to-end digital submissions and improvements to

Qualifications

• 7+ years of statistical programming experience in pharma/biopharma
• Fluent in SAS and CDISC SDTM/ADaM standards
• Experience with end-to-end clinical data lifecycle and regulatory submissions

Responsabilités

• Turn complex clinical data into submission-ready outputs for regulators
• Design and implement technical solutions that influence product advancement
• Collaborate with statisticians, data managers, and external vendors in cross-functional teams

Connaissances

SAS

CDISC standards

ADaM specifications

Statistics knowledge

Formation

Statistics/ Biostatistics/ Mathematics / CS / Life Sciences degree

Outils

Electronic submissions experience

Description du poste

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 helped save a life?

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.

So, what will you actually be doing?

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.

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.

And if you're the kind of person who sees a broken process and immediately starts thinking about how to fix it? You'll have the platform and the influence to actually do something about it here.

What's in it for you - really?

Let's be direct about the tangible value this role brings to your career:

• 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 at BMS. If you have ideas, there's a culture here that wants to hear them.

You'll thrive here if you...

• 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.

Why BMS?

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.

Ready to write code that changes lives - apply today.

#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 [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/

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If this posting is missing required information required by local law or incorrect, contact BMS at [e-mail] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1607142 : Principal Statistical Programmer