At a Glance
- Tasks: Write and validate SAS programs to generate clinical datasets and reports.
- Company: Join a leading global biopharmaceutical company focused on life-changing medicines.
- Benefits: Competitive salary, flexible work options, and opportunities for professional growth.
- Other info: Collaborative culture with a focus on innovation and efficiency.
- Why this job: Make a real impact on medicine development and regulatory decisions.
- Qualifications: Bachelor's degree in relevant fields and experience in statistical programming.
The predicted salary is between 50000 - 65000 £ per year.
You'll be a key technical voice within our Global Biometrics & Data Sciences (GBDS) function, working closely with cross‑functional clinical teams, collaborating with external vendors, and owning your programming workload with real autonomy. This is a focused individual contributor role – no line management responsibilities – so you can put your energy exactly where it matters most: delivering high‑quality, high‑impact programming work.
Day to day, that looks like:
- Writing and validating SAS programs to generate derived analysis datasets and clinical Tables, Figures, and Listings (TFLs) – work that feeds directly into regulatory decision‑making.
- Contributing to electronic submission preparation (NDA, BLA, MAA) – real regulatory milestones that mark pivotal moments in a medicine's journey.
- Reviewing and shaping key planning documents such as Statistical Analysis Plans (SAPs) and Data Presentation Plans – ensuring clarity and completeness before programming work begins, your input genuinely steers project direction.
- Partnering with vendors on programming standards, specifications, and file transfers – building collaborative relationships that make complex programmes run smoothly.
- Independently leading programming assignments across multiple projects with minimal supervision – you have real ownership and the trust that accompanies it.
- Spotting opportunities to improve efficiency and consistency across GBDS, contributing to initiatives that make the whole team better, and exposure to the full clinical development lifecycle, from data collection through regulatory submission.
- The chance to work with industry‑leading standards and technologies in a global biometrics function.
- A culture that actively encourages you to identify improvements and champion change – your ideas won’t gather dust here.
- Collaboration with talented, purpose‑driven colleagues across global cross‑functional teams.
Qualifications:
- A Bachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences.
- Demonstrated industry experience in statistical programming.
Core Skills & Knowledge:
- Strong, proven proficiency in SAS for producing derived analysis datasets and TFLs.
- In‑depth understanding of clinical data structures, including CDISC standards (SDTM, ADaM) and relational databases.
- Hands‑on experience with upstream data handling – multiple data forms, eDC, workflow, and SDTM.
- Ability to deliver downstream outputs including ADaM datasets, Data Definition Tables, and e‑submission packages.
- Confidence with tools such as MS Office, XML, and Pinnacle 21.
- A solid grasp of regulatory, industry, and technology standards – you understand why the rules exist, not just what they are.
- Familiarity with statistical terminology, clinical trial methodology, medical terminology, and protocol designs.
- A genuine team player – you communicate well, build bridges across functions, and make the people around you more effective.
Preferred Credentials:
- Deep experience supporting global regulatory filings (NDA, BLA, MAA) within pharma clinical development.
- Broad knowledge of the end‑to‑end drug development process and global regulatory frameworks.
- Experience with R or other statistical programming languages.
- Familiarity with the Linux operating system.
As our Senior Statistical Programmer, you are one of the people who turns clinical data into life‑changing decisions. Your programming expertise directly shapes how new medicines are developed, reviewed by regulators, and ultimately approved for patients worldwide.
Senior Statistical Programmer in Denham employer: Bristol-Myers Squibb Company
At our company, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to take ownership of their projects. As a Senior Statistical Programmer, you will enjoy the autonomy to make impactful contributions while working alongside talented colleagues in a global biometrics function. With a strong emphasis on professional growth and the opportunity to influence key regulatory milestones, we offer a rewarding environment where your ideas are valued and can lead to meaningful advancements in medicine.
Contact Details:
Bristol-Myers Squibb Company Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Senior Statistical Programmer in Denham
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to statistical programming. We recommend doing mock interviews with friends or colleagues to build your confidence and refine your answers. Remember, showing your expertise in SAS and clinical data structures is key!
✨Tip Number 3
Don’t forget to showcase your projects! Whether it’s through a portfolio or discussing past experiences during interviews, we want to see how you’ve applied your skills in real-world situations. Highlighting your contributions to regulatory submissions can really set you apart.
✨Tip Number 4
Apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows your genuine interest in joining our team at StudySmarter. Let’s make those high-impact programming dreams a reality together!
We think you need these skills to ace Senior Statistical Programmer in Denham
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that match the Senior Statistical Programmer role. Highlight your proficiency in SAS and any relevant experience with clinical data structures, as this will show us you’re the right fit for the job.
Craft a Compelling Cover Letter:Use your cover letter to tell us why you're passionate about statistical programming and how your background aligns with our mission at StudySmarter. Share specific examples of your work that demonstrate your ability to deliver high-quality programming outputs.
Showcase Your Collaboration Skills:Since this role involves working closely with cross-functional teams and external vendors, make sure to highlight your teamwork and communication skills. We want to see how you’ve successfully partnered with others to achieve project goals.
Apply Through Our Website:Don’t forget to submit your application through our website! It’s the best way for us to receive your materials and ensures you’re considered for the role. Plus, it shows us you’re keen on joining the StudySmarter team!
How to prepare for a job interview at Bristol-Myers Squibb Company
✨Know Your SAS Inside Out
Make sure you brush up on your SAS programming skills before the interview. Be ready to discuss specific projects where you've used SAS to generate analysis datasets and TFLs. Highlight any challenges you faced and how you overcame them, as this shows your problem-solving abilities.
✨Understand Clinical Data Structures
Familiarise yourself with CDISC standards and clinical data structures. During the interview, be prepared to explain how these standards impact your programming work. This will demonstrate your in-depth understanding of the field and your ability to contribute effectively from day one.
✨Showcase Your Collaboration Skills
Since this role involves working closely with cross-functional teams and external vendors, think of examples that showcase your teamwork and communication skills. Discuss how you've built relationships in past roles and how that has led to successful project outcomes.
✨Be Ready to Discuss Regulatory Knowledge
Brush up on your knowledge of regulatory submissions like NDA, BLA, and MAA. Be prepared to talk about your experience with electronic submission preparation and how you ensure compliance with industry standards. This will show that you understand the importance of your role in the broader context of drug development.
