Statistical Programmer in Denham

Working with Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams.

Bristol Myers Squibb recognises the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Hybrid Working - 50% Onsite

Your Code Could Help Save a Life. At Bristol Myers Squibb, the programs you write, the datasets you build, and the outputs you validate feed directly into the regulatory submissions that bring new medicines to patients who need them most. This isn't just a programming job. It's a chance to sit at the intersection of data science and drug development - where your technical precision has a real, measurable impact on clinical outcomes around the world.

What Your Day-to-Day Actually Looks Like:

• You’ll be embedded within our Global Biometrics & Data Sciences (GBDS) team, working closely with clinical project teams, external vendors, and cross-functional colleagues across the full drug development lifecycle.
• Writing and validating SAS/R programs to produce derived analysis datasets and the tables, listings, and figures (TFLs) that underpin clinical evidence — knowing that every output you produce is held to the highest standard of accuracy.
• Contributing to regulatory submissions (think NDAs, BLAs, MAAs) - this is your chance to be part of the team that gets a medicine over the line.
• Reviewing key planning documents like Statistical Analysis Plans, so you're always connected to the bigger picture and can anticipate exactly what's needed before it's needed.
• Leading programming assignments independently across multiple projects - you'll have real ownership here, not just task tickets.
• Spotting and driving efficiencies - if you see a smarter way to do something, we want to hear it.

What You Bring To The Table:

• A Bachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science or a Life Sciences discipline.
• At least 2 years of industry programming experience.
• Solid, demonstrable proficiency in SAS for producing derived datasets and TFLs.
• A firm grasp of CDISC standards, clinical data structures, and relational databases.
• Hands-on experience with SDTM, ADaM, Data Definition Tables and e-submissions.
• Familiarity with tools like Pinnacle 21, XML, and MS Office.
• A working knowledge of regulatory and industry standards - you understand the rules and the reasons behind them.

Bonus Points If You Have:

• Experience supporting regulatory filings (NDA, BLA or MAA) within a pharma environment.
• Comfort working with R or R-Shiny.
• Exposure to real-world data or real-world evidence.

Why BMS — And Why Now?

• The work matters. BMS has a pipeline of innovative therapies in oncology, immunology, and cardiovascular disease.
• You’ll grow. With exposure to global regulatory submissions, cutting-edge data standards, and a collaborative team that spans the globe, this role is a genuine accelerator for your career in clinical programming.
• You’ll have balance. Our hybrid model means 50% of your time is onsite in our modern Uxbridge office.
• You’ll be heard. We actively encourage our programmers to identify efficiency gains and contribute to improvement initiatives.

Uniquely Interesting Work, Life-changing Careers. With a single vision as inspiring as “Transforming patients’ lives through science™”, every BMS employee plays an integral role in work that goes far beyond ordinary.