Senior Statistical Programmer GB R1602748 Posted ago

Position: Senior Statistical Programmer GB R1602748 Posted 18 hours ago
## Senior Statistical Programmer Uxbridge - GBFind out how well you match with this job
** 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:
** 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
** We're looking for someone with a solid foundation and the drive to apply it meaningfully. Here's what we need:
** 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…