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About the Role
As a Senior Statistical Programmer at Bristol Myers Squibb, you will play a crucial role in transforming clinical data into life-changing decisions. Your programming expertise will directly shape how new medicines are developed, reviewed by regulators, and approved for patients worldwide. This is a focused individual contributor role where you will be a key technical voice within the Global Biometrics & Data Sciences (GBDS) function, collaborating with cross-functional clinical teams and external vendors.
Responsibilities
- Writing and validating SAS programs to generate derived analysis datasets and clinical Tables, Figures, and Listings (TFLs).
- Contributing to electronic submission preparation (NDA, BLA, MAA).
- Reviewing and shaping key planning documents like Statistical Analysis Plans (SAPs) and Data Presentation Plans.
- Partnering with vendors on programming standards, specifications, and file transfers.
- Independently leading programming assignments across multiple projects with minimal supervision.
- Spotting opportunities to improve efficiency and consistency across GBDS, contributing to team-wide initiatives.
Requirements
- A 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 with strong communication skills.
Skills
- SAS programming
- CDISC standards (SDTM, ADaM)
- Relational databases
- Upstream data handling
- eDC
- SDTM
- ADaM datasets
- Data Definition Tables
- e-submission packages
- MS Office
- XML
- Pinnacle 21
- Regulatory standards
- Industry standards
- Technology standards
- Statistical terminology
- Clinical trial methodology
- Medical terminology
- Protocol designs
- Global regulatory filings (NDA, BLA, MAA)
- Drug development process
- Global regulatory frameworks
- R
- Linux operating system
Location
- Uxbridge, UK
Work Type
- Hybrid Working: 50% Onsite
Experience Level
- Senior
Education Level
- Bachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences
Benefits
- Opportunities for growth
- Supportive environment
- Inclusion
- Wellbeing
- Flexibility
- Comprehensive benefits
- Exposure to the full clinical development lifecycle
- Chance to work with industry-leading standards and technologies
- Culture that actively encourages identifying improvements and championing change
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.
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.