Senior Statistical Programmer - Hybrid Submissions

Bristol Myers Squibb; Uxbridge; Hybrid; GBP 90,000 - 120,000; Full time

Job summary

Bristol Myers Squibb in the United Kingdom is seeking a Principal Statistical Programmer to lead data programming for pivotal trials and regulatory submissions. You will transform complex clinical data into submission-ready outputs and influence cross-functional teams.

The role emphasizes SAS, CDISC standards (SDTM/ADaM) and end-to-end data pipelines, with hybrid work and global trial exposure to drive patient outcomes.

Qualifications

• 7+ years of statistical programming experience in pharma/biopharma.
• Fluent in SAS, CDISC/SDTM/ADaM standards and end-to-end data pipeline.
• Experience with regulatory submissions and life-cycle documentation.

Responsibilities

• Lead electronic submissions for regulatory filings.
• Design and implement programming strategies for trials.
• Collaborate with statisticians, data managers and external vendors.

Skills

SAS programming

CDISC/SDTM/ADaM

Regulatory submissions

Education

Statistics/ Biostatistics degree

Tools

ADaM specifications

Job description

Bristol Myers Squibb in the United Kingdom is seeking a Principal Statistical Programmer to lead data programming for pivotal trials and regulatory submissions. You will transform complex clinical data into submission-ready outputs and influence cross-functional teams.

The role emphasizes SAS, CDISC standards (SDTM/ADaM) and end-to-end data pipelines, with hybrid work and global trial exposure to drive patient outcomes.