Principal Statistical Programmer

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at 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. Take your career farther than you thought possible. Bristol Myers Squibb recognizes 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. Read more: . 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 If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. 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. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. 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 . Visit 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 for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. 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 . Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley. R1604796 : Principal Statistical Programmer