Senior SDTM Statistical Programmer

At Bristol Myers Squibb our employees often ask Who are you working fora 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.

Location: Uxbridge UK

Hybrid Working: 50% Onsite

Your code doesnt just run. It helps get life-changing medicines to patients.

At Bristol Myers Squibb we believe that behind every clean dataset every validated submission package every regulatory approval - theres a person who made it possible. That person could be you.

Were looking for aSenior SDTM Statistical Programmerto join our team - someone whos ready to stop justdeliveringwork and start genuinelyleadingit.

So what does this actually mean for you

• Youll own something that matters - This isnt a role where youre handed a ticket and told to close it. Youll be thetechnical leadon assigned studies - shaping SDTM strategies from protocol review all the way through to global regulatory submission. Youll see the full picture and your fingerprints will be on deliverables that directly support medicines reaching patients around the world.
• Youll solve real complex problems - not just tick boxes - Root cause analysis cross-functional stakeholder collaboration data integration from CRF and non-CRF sources - this role puts you at the intersection ofscience data and process. Youll build the kind of deep end-to-end understanding that makes you genuinely invaluable not just technically but strategically.
• Youll be at the frontier of where the industry is going - SDTM automation. Metadata-driven processes. Agentic AI workflows. These arent buzzwords here - theyre part of how were transforming clinical data operations. Youll be actively engaged withemerging technologies keeping your skills sharp and future-proof in a field thats evolving fast.
• Youll lead people not just processes - Youll provide guidance and quality oversight to team members and manage CRO and vendor programming activities. Whether its mentoring a junior programmer or partnering with a cross-functional study team youll develop the kind ofleadership presencethat accelerates careers - yours included.
• Youll contribute to global regulatory success - Every eCRT submission package you build every Pinnacle 21 validation report you interpret every SDTM specification you design it all feeds intoglobal regulatory filings and approvals. Few roles let you see your technical work translate so directly into real-world impact.

What youll bring to the table

• 4 yearsof pharmaceutical or CRO experience as a SAS Programmer supporting clinical trials and regulatory submissions
• Deep expertise inCDISC/SDTM standardsand a thorough understanding of the clinical development lifecycle
• Exceptional SAS programming skills (Base Stat Graph) and comfort working across complex multi-source data environments
• Experience collaborating with cross-functional teams managing timelines and driving quality outcomes
• A degree in a relevant scientific discipline (BA/BS or above)
• The agility to adapt quickly prioritise effectively and lead through ambiguity because clinical development rarely stands still

Why BMS

Because here your work is more than a deliverable. Its part of a mission totransform patients lives through science. Youll work alongside some of the most talented minds in the industry supported by a culture that values innovation collaboration and the courage to take on the hardest problems in medicine.

Youll grow your technical expertise build your leadership profile and know with certainty that what you do every day genuinely matters.

Ready to lead from the data up

Apply now and bring your SDTM expertise to work that changes lives

#LI-Hybrid

We hire for skills and capabilities not just credentials if this role excites you but doesnt 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 People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process reasonable workplaceaccommodations/adjustmentsand ongoing support in their roles. Applicants can request a reasonable workplaceaccommodation/adjustmentprior to accepting a job offer. If you require reasonableaccommodations/adjustmentsin completing this application or in any part of the recruitment process direct your inquiries to. Visit access our complete Equal Employment Opportunity statement.

Bristol Myers Squibb is Disability Confident Employer

A UK Government scheme

Candidate Rights

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