SDTM Operations and Programming

Working with Us
Challenging. Meaningful. Life-changing. Those arent 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. Youll 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: code doesnt just run. It helps get life-changing medicines to patients.

At Bristol Myers Squibb we believe that behind every clean dataset every validated submission package every regulatory approval - theres a person who made it possible. That person could be you.

Were looking for aSenior SDTM Statistical Programmerto join our team - someone whos ready to stop justdeliveringwork and start genuinelyleadingit.

So what does this actually mean for you

• Youll own something that matters - This isnt a role where youre handed a ticket and told to close it. Youll be thetechnical leadon assigned studies - shaping SDTM strategies from protocol review all the way through to global regulatory submission. Youll see the full picture and your fingerprints will be on deliverables that directly support medicines reaching patients around the world.
• Youll solve real complex problems - not just tick boxes - Root cause analysis cross-functional stakeholder collaboration data integration from CRF and non-CRF sources - this role puts you at the intersection ofscience data and process. Youll build the kind of deep end-to-end understanding that makes you genuinely invaluable not just technically but strategically.
• Youll be at the frontier of where the industry is going - SDTM automation. Metadata-driven processes. Agentic AI workflows. These arent buzzwords here - theyre part of how were transforming clinical data operations. Youll be actively engaged withemerging technologies keeping your skills sharp and future-proof in a field thats evolving fast.
• Youll lead people not just processes - Youll provide guidance and quality oversight to team members and manage CRO and vendor programming activities. Whether its mentoring a junior programmer or partnering with a cross-functional study team youll develop the kind ofleadership presencethat accelerates careers - yours included.
• Youll contribute to global regulatory success - Every eCRT submission package you build every Pinnacle 21 validation report you interpret every SDTM specification you design it all feeds intoglobal regulatory filings and approvals. Few roles let you see your technical work translate so directly into real-world impact.

What youll bring to the table

• 4 yearsof pharmaceutical or CRO experience as a SAS Programmer supporting clinical trials and regulatory submissions
• Deep expertise inCDISC/SDTM standardsand a thorough understanding of the clinical development lifecycle
• Exceptional SAS programming skills (Base Stat Graph) and comfort working across complex multi-source data environments
• Experience collaborating with cross-functional teams managing timelines and driving quality outcomes
• A degree in a relevant scientific discipline (BA/BS or above)
• The agility to adapt quickly prioritise effectively and lead through ambiguity because clinical development rarely stands still

Why BMS

Because here your work is more than a deliverable. Its part of a mission totransform patients lives through science. Youll work alongside some of the most talented minds in the industry supported by a culture that values innovation collaboration and the courage to take on the hardest problems in medicine.

Youll grow your technical expertise build your leadership profile and know with certainty that what you do every day genuinely matters.

Ready to lead from the data up

Apply now and bring your SDTM expertise to work that changes lives

#LI-Hybrid

If you come across a role that intrigues you but doesnt perfectly line up with your resume we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work Life-changing Careers
With a single vision as inspiring as Transforming patients lives through science every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture promoting global participation in clinical trials while our shared values of passion innovation urgency accountability inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential site-by-design field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles onsite presence is considered an essential job function and is critical to collaboration innovation productivity and a positive Company culture. For field-based and remote-by-design roles the 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.

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 . Visit to access our complete Equal Employment Opportunity statement.

Bristol Myers Squibb is Disability Confident Employer

A UK Government scheme

Candidate Rights

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

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 data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.