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About the Role

Join Bristol Myers Squibb as a Senior SDTM Statistical Programmer, a purpose-driven role where your technical leadership will directly contribute to delivering innovative medicines to patients. This position offers the opportunity to shape SDTM strategies, solve complex data challenges, and work with emerging technologies in clinical data operations.

Responsibilities

Serve as the technical lead on assigned studies, shaping SDTM strategies from protocol review to global regulatory submission.
Perform root cause analysis and collaborate with cross-functional stakeholders.
Integrate data from CRF and non-CRF sources.
Engage with emerging technologies such as SDTM automation, metadata-driven processes, and agentic AI workflows.
Provide guidance and quality oversight to team members.
Manage CRO and vendor programming activities.
Build eCRT submission packages.
Interpret Pinnacle 21 validation reports.
Design SDTM specifications.

Requirements

4+ years of pharmaceutical or CRO experience as a SAS Programmer supporting clinical trials and regulatory submissions.
Deep expertise in CDISC/SDTM standards.
Thorough understanding of the clinical development lifecycle.
Exceptional SAS programming skills (Base, Stat, Graph).
Comfort working across complex, multi-source data environments.
Experience collaborating with cross-functional teams.
Experience managing timelines.
Experience driving quality outcomes.
Agility to adapt quickly, prioritize effectively, and lead through ambiguity.

Skills

SAS programming (Base, Stat, Graph)
CDISC/SDTM standards
Data integration
Root cause analysis
Cross-functional collaboration
SDTM automation
Metadata-driven processes
Agentic AI workflows
Pinnacle 21 validation

Location

Uxbridge, UK

Work Type

Hybrid Working: 50% Onsite

Experience Level

Senior

Education Level

Degree in a relevant scientific discipline (BA/BS or above)

Benefits

Opportunities for growth
Supportive environment
Inclusion
Wellbeing
Flexibility
Comprehensive benefits

About the Company

Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
We believe that behind every clean dataset, every validated submission package, every regulatory approval - there's a person who made it possible.
We hire for skills and capabilities, not just credentials.
Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design.

Equal Opportunity

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.
Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Bristol Myers Squibb is Disability Confident – Employer
BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.