Principal Statistical Programmer

Bristol Myers Squibb EU Policy; Uxbridge; Hybrid; GBP 90,000 - 130,000; Full time

Job summary

Bristol Myers Squibb in the UK is seeking a Principal Statistical Programmer to join our regulatory programming team. You will translate complex clinical data into submission-ready outputs and influence regulatory filings.

You’ll review analysis plans, shape programming strategy, and advise senior stakeholders on risk and resolution. This role offers a path to leadership within a global oncology/biopharma environment.

Qualifications

• 7+ years of statistical programming experience in the pharmaceutical or biopharma industry, including hands-on involvement in major regulatory submissions.
• Fluent in SAS, CDISC/SDTM/ADaM standards, and the end-to-end clinical data pipeline.
• Understanding of the full drug development lifecycle—from eDC data collection to TFLs and e-submission components.
• Ability to operate in cross-functional teams with statisticians, clinicians, and regulatory experts.
• Proactive at spotting problems before they escalate and able to communicate clearly.
• Degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences.

Responsibilities

• Lead electronic submissions for significant regulatory filings and contribute to clinical package preparation.
• Review analysis plans, shape programming strategy, and advise senior stakeholders on risk and resolution.
• Mentor and develop other programming professionals and build a high-performing team.

Skills

Statistical programming

Regulatory submissions

SAS

CDISC/SDTM/ADaM

Data pipeline understanding

Team leadership

Education

Degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences

Tools

SAS

CDISC/SDTM/ADaM

Job description

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: careers.bms.com/working-with-us.

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.

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.

What's in it for you - really?

• 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.

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 [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 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 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 you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at [e-mail]. 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