Senior Statistical Programmer

Bristol Myers Squibb; Denham; Hybrid; GBP 65,000 - 90,000; Full time

Job summary

Bristol Myers Squibb in Uxbridge, UK, is seeking a Senior Statistical Programmer in a hybrid role with 50% onsite work. You will lead SAS programming for derived analysis datasets, TFLs, and regulatory deliverables, while collaborating across the Global Biometrics & Data Sciences function.

The role emphasizes ownership of programming work, interaction with cross-functional clinical teams, and contribution to regulatory submissions and data standards as part of a world-class pharmacovigilance and

Qualifications

• Bachelor’s degree in Statistics/Biostatistics/Math/CS/Life Sciences.
• Industry experience in statistical programming.
• Knowledge of SDTM/ADaM standards and clinical data structures.
• Regulatory submission experience is advantageous.

Responsibilities

• Write and validate SAS programs to generate derived analysis datasets and TFLs.
• Support NDA, BLA, MAA submissions and regulatory milestones.
• Review SAPs and Data Presentation Plans before programming work begins.
• Collaborate with vendors on standards, specifications and file transfers.
• Independently lead programming assignments across multiple projects with limited supervision.
• Identify opportunities to improve GBDS efficiency and consistency.

Skills

SAS Proficiency

SDTM/ADaM

Data Handling

Regulatory Submissions

Education

Bachelor's degree in Statistics/Biostatistics/Math/CS/Life Sciences

Experience in statistical programming

Tools

MS Office

XML

Pinnacle 21

Linux

Job description

Location: Uxbridge, UK

Hybrid Working: 50% Onsite

Are you ready to turn clinical data into life-changing decisions?

At Bristol Myers Squibb, we believe that behind every dataset, every line of code, and every submission package, there's a patient waiting for a better option. As our Senior Statistical Programmer, you are one of the people who makes that happen.

This isn't a role where your work disappears into a black box. Here, your programming expertise directly shapes how new medicines are developed, reviewed by regulators, and ultimately approved for patients around the world. That's a pretty remarkable thing to be part of.

What You'll Actually Be Doing

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 (think NDA, BLA, MAA) — real regulatory milestones that mark pivotal moments in a medicine's journey
• Reviewing and shaping key planning documents like 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 the kind of collaborative relationships that make complex programmes run smoothly
• Independently leading programming assignments across multiple projects with minimal supervision - you'll have real ownership and the trust to match it
• Spotting opportunities to improve efficiency and consistency across GBDS, contributing to initiatives that make the whole team better

What You Bring To The Table

Education & Background

• 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 like 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

It’d be a bonus if you also have…

• 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

Why this role, why BMS, why now?

Here, your skills aren't just technically valued - they're mission critical. You'll work in an environment that respects your expertise, gives you the autonomy to lead your own work, and connects your daily output to outcomes that genuinely matter.

You'll Gain

• Exposure to the full clinical development lifecycle, from data collection through to 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

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t 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 https://careers.bms.com/ways-of-working.

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

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

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 this posting is missing required information required by local law or incorrect, contact BMS at [e-mail] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1604799 : Senior Statistical Programmer