At a Glance
- Tasks: Lead SDTM strategies and ensure data integrity for life-changing medicines.
- Company: Bristol Myers Squibb, a purpose-driven pharmaceutical company.
- Benefits: Hybrid working, comprehensive benefits, and opportunities for personal growth.
- Other info: Join a collaborative culture that values inclusion and innovation.
- Why this job: Make a real impact on patients' lives through innovative data solutions.
- Qualifications: 4+ years in SAS programming with expertise in CDISC/SDTM standards.
The predicted salary is between 59400 - 72600 £ per year.
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.
Location: Uxbridge, UK
Hybrid Working: 50% Onsite
Your code doesn't 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 - there's a person who made it possible. That person could be you. We're looking for a Senior SDTM Statistical Programmer to join our team - someone who's ready to stop just delivering work and start genuinely leading it.
So, what does this actually mean for you?
- You'll own something that matters - This isn't a role where you're handed a ticket and told to close it. You'll be the technical lead on assigned studies - shaping SDTM strategies from protocol review all the way through to global regulatory submission. You'll see the full picture and your fingerprints will be on deliverables that directly support medicines reaching patients around the world.
- You'll 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 of science, data, and process. You'll build the kind of deep, end-to-end understanding that makes you genuinely invaluable, not just technically but strategically.
- You'll be at the frontier of where the industry is going - SDTM automation. Metadata-driven processes. Agentic AI workflows. These aren't buzzwords here - they're part of how we're transforming clinical data operations. You'll be actively engaged with emerging technologies, keeping your skills sharp and future-proof in a field that's evolving fast.
- You'll lead people, not just processes - You'll provide guidance and quality oversight to team members and manage CRO and vendor programming activities. Whether it's mentoring a junior programmer or partnering with a cross-functional study team, you'll develop the kind of leadership presence that accelerates careers - yours included.
- You'll 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 into global regulatory filings and approvals. Few roles let you see your technical work translate so directly into real-world impact.
What you'll bring to the table:
- 4+ years of pharmaceutical or CRO experience as a SAS Programmer supporting clinical trials and regulatory submissions
- Deep expertise in CDISC/SDTM standards and 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. It's part of a mission to transform patients' lives through science. You'll 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. You'll 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.
Senior SDTM Statistical Programmer in Denham employer: Bristol-Myers Squibb Co
Bristol Myers Squibb is an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation. As a Strategic Country Controller for Switzerland & Austria, you will benefit from extensive professional growth opportunities while working in a supportive environment that values integrity and excellence. With the chance to engage with global finance teams and contribute to impactful financial strategies, this role provides a meaningful career path in a leading biopharmaceutical company.
StudySmarter Expert Advice🤫
We think this is how you could land Senior SDTM Statistical Programmer in Denham
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Bristol-Myers Squibb Co. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Bristol-Myers Squibb Co.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Bristol-Myers Squibb Co. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Bristol-Myers Squibb Co is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Senior SDTM Statistical Programmer in Denham
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Bristol-Myers Squibb Co!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Bristol-Myers Squibb Co that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Bristol-Myers Squibb Co!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Bristol-Myers Squibb Co, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Bristol-Myers Squibb Co
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Bristol-Myers Squibb Co that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Bristol-Myers Squibb Co’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
