Bristol Myers Squibb

SeniorStatisticalProgrammer

United Kingdom FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Senior Statistical Programmer at Bristol Myers Squibb. Skills: SAS, Statistical programming, Clinical data, Regulatory submissions. Write and validate SAS programs. Generate derived analysis datasets”

What You'll Achieve.

Deliver high-quality, high-impact programming work; Generate derived analysis datasets and clinical Tables, Figures, and Listings (TFLs); Contribute to electronic submission preparation; Deliver downstream outputs including ADaM datasets, Data Definition Tables, and e-submission packages; Transforming patients’ lives through science

What They're Looking For.

Must Have

Bachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences, Demonstrated industry experience in statistical programming, 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, 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

Nice to 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

What You'll Do.

Write and validate SAS programs

Generate derived analysis datasets

Generate clinical Tables

Contribute to electronic submission preparation

Review and shape planning documents

Partner with vendors on programming standards

Lead programming assignments

Improve efficiency and consistency

How You'll Work.

Team & Collaboration

Work closely with cross-functional clinical teams; Collaborate with external vendors; Partner with vendors on programming standards; Build collaborative relationships; Communicate well; Build bridges across functions; Make people around you more effective; Collaboration with talented, purpose-driven colleagues

Communication Scope

Communicate well

Process & Methodology

Own programming workload, Independently lead programming assignments

Full 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](https://careers.bms.com/working-with-us). **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: deliveri

Free ATS check

Applying for this Senior Statistical Programmer role?

Most applicants get filtered before a human reads their resume. See if yours makes the cut.

How to Apply on Workday

  • Workday has a multi-step form — save your progress after every section.
  • "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
  • Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
  • Job requisition numbers are useful when following up with HR by email.

ANONYMOUS · UNFILTERED

What do employees actually say about Bristol Myers Squibb?

Real rants from real employees. Read before you apply.

Read Company Rants →