BMS Business Services Ltd Posted September 1, 2026

Principal Statistical Programmer

Uxbridge, United Kingdom Full time
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BMS Business Services Ltd is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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  adastaffingsupport@bms.com . 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.

If this posting is missing required information required by local law or incorrect, contact BMS at  TAEnablement@bms.com 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.

R1604796 : Principal Statistical Programmer

Job details

Seniority
Principal
Function
Clinical Development
Therapeutic area
Not listed
Location
Uxbridge, United Kingdom
Employment type
Full time

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 313 comparable Principal Clinical Development roles across 58 biopharma companies.

313Comparable roles tracked
286Currently active
58Companies hiring similar roles
19Countries represented

Salary context

129 of 313 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Peer group range $96,200 – $392,100 (median $255,000)

Where these roles are based

Top locations among the 313 comparable roles

United States195
India54
United Kingdom17
Switzerland8
Spain8
Germany5

+ 13 more countries

Seniority mix

313 of 313 peers have a known seniority level

Director191
Senior103
Principal19

Therapeutic area mix

75 of 313 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology35
Neuroscience17
Immunology8
Cardiovascular / CVRM6
Ophthalmology4
Respiratory3
Rare Disease2

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Mylan Pharma UK Limited Sandwich, United Kingdom Principal
Same function Same seniority Same country
60%similar
Ipsen Biopharm Ltd London (UK), United Kingdom Principal
Same function Same seniority Same country
60%similar
BMS Business Services Ltd Uxbridge, United Kingdom Principal
Same function Same seniority Same country
50%similar
Novartis London (The Westworks), United Kingdom Director
Same function Adjacent seniority Same country
50%similar
Novartis London (The Westworks), United Kingdom Director
Same function Adjacent seniority Same country
50%similar
Novartis London (The Westworks), United Kingdom Director
Same function Adjacent seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Principal Statistician
Mylan Pharma UK Limited · Sandwich, United Kingdom · Principal
Function Therapeutic area Seniority Country
50%
Senior Clinical Development Medical Director
Novartis · London (The Westworks), United Kingdom · Director
Function Therapeutic area Adjacent seniority Country
50%
Senior Medical Director Early Clinical Respiratory
AstraZeneca · Cambridge, United Kingdom · Director
Function Therapeutic area Adjacent seniority Country
50%
Clinical Development Medical Director, Autoimmune/Rare Diseases
Vertex UK Int'l HQ/R&D · Paddington, United Kingdom · Director
Function Therapeutic area Adjacent seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.