Bristol Myers Squibb

pharmaceutical

SeniorManager,StatisticalProgramming

United Kingdom FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Senior Manager, Statistical Programming at Bristol Myers Squibb. Skills: SAS programming, CDISC standards, ADaM specifications, electronic submissions. programming expert that clinical project teams rely on. design and implement technical solutions that directly influence whether a medicine moves forward”

What You'll Achieve.

submission-ready outputs that regulators trust; technical decisions will have a direct line to patient outcomes; career-defining experience

Industry & Context.

pharmaceutical
Problems you'll solve

takes complex, messy clinical data and turns it into clear, submission-ready outputs; proactive about spotting problems _before_ they become crises

Eligibility Requirements

ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function

What They're Looking For.

Must Have

7 + years of statistical programming experience in the pharmaceutical or biopharma industry, hands-on involvement in major regulatory submissions, deeply fluent in SAS, CDISC/SDTM/ADaM standards, understanding the full drug development lifecycle — from eDC data collection through to TFLs and e-submission components, proactive about spotting problems _before_ they become crises — and confident enough to communicate them clearly

Nice to Have

led or managed a team of technical professionals

What You'll Do.

programming expert that clinical project teams rely on

design and implement technical solutions that directly influence whether a medicine moves forward

lead and support electronic submissions for significant regulatory filings

review statistical analysis plans

shape programming strategy

advise senior stakeholders on risk and resolution

and develop other technical professionals

help talented programmers grow

identify inefficiencies

lead improvement initiatives

influence the future of how statistical programming operates at BMS

How You'll Work.

Team & Collaboration

embedded in cross-functional teams; partnering with statisticians, data managers, clinical scientists, and external vendors; building relationships across Bristol Myers Squibb's Global Biometrics & Data Sciences (GBDS) organisation and beyond

Communication Scope

communicate problems clearly

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). **What if your code helped save a life?** It sounds dramatic — but that's exactly what's at stake here. At Bristol Myers Squibb, we're in the business of discovering, developing, and delivering medicines that genuinely change patients' lives. And behind every successful clinical trial, every regulatory submission, every approved therapy? There's a team of brilliant statistical programmers making sure the data tells the right story, accurately, compliantly, and on time. _**That 's where you come in.**_ **So, what will you actually be doing?** You'll be the programming expert that clinical project teams rely on. The person who takes complex, messy clinical data and turns it into clear, submission-ready outputs that regulators trust. You'll design and implement technical solutions that directly influence whether a medicine moves forward — or doesn't. That means working with **CDISC standards, ADaM specifications, SAS programming, and electronic submissions** — things you already know inside and out. But it also means something

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