Hybrid Senior Statistical Programmer - Submissions Expert

Bristol-Myers Squibb; Uxbridge; Hybrid; GBP 70,000 - 110,000; Full time

Job summary

Bristol Myers Squibb in the United Kingdom is seeking a Senior Statistical Programmer to join cross-functional teams delivering submission-ready outputs that regulators trust. You’ll work with CDISC/SDTM/ADaM standards, SAS programming, and the end-to-end data pipeline to influence regulatory filings and patient outcomes, embedded in GBDS across global teams.

Experience of 7+ years in pharma/biopharma and a degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences are

Qualifications

• 7+ years of statistical programming experience in pharma/biopharma.
• Fluent with SAS, CDISC/SDTM/ADaM standards and end-to-end clinical data pipeline.
• Able to collaborate with statisticians, data managers, clinicians and regulators.

Responsibilities

• Lead and support electronic submissions for significant regulatory filings.
• Review SAPs, shape programming strategy and advise senior stakeholders on risk and resolution.
• Mentor and develop other technical professionals within the team.

Skills

Statistical programming

SAS

CDISC/SDTM/ADaM

Cross-functional collaboration

Regulatory submissions

Problem solving

Education

Statistics/Biostatistics/Mathematics/CS/Life Sciences degree

Tools

SAS

Job description

Bristol Myers Squibb in the United Kingdom is seeking a Senior Statistical Programmer to join cross-functional teams delivering submission-ready outputs that regulators trust. You’ll work with CDISC/SDTM/ADaM standards, SAS programming, and the end-to-end data pipeline to influence regulatory filings and patient outcomes, embedded in GBDS across global teams.

Experience of 7+ years in pharma/biopharma and a degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences are