Senior Statistical Programmer – Hybrid, Submissions

Bristol-Myers Squibb; Uxbridge; Hybrid; GBP 70,000 - 100,000; Full time

Benefits offered by this job

50% Hybrid Working

Hybrid work model in Uxbridge

Job summary

Bristol Myers Squibb is seeking a Principal Statistical Programmer in Uxbridge to join our GBDS team. You will transform complex clinical data into submission-ready outputs, working with cross-functional teams to influence regulatory decisions and patient outcomes.

You will design technical solutions using SAS and CDISC standards, contribute to SAS programming strategies, and participate in end-to-end data pipelines for major trials in a hybrid UK setting.

Qualifications

• 7+ years of statistical programming experience in the pharmaceutical/biopharma industry.
• Fluent in SAS and CDISC/SDTM/ADaM standards and the end-to-end clinical data pipeline.
• Understand the drug development lifecycle from data capture to e-submission components.

Responsibilities

• You will be the programming expert relied upon by clinical project teams.
• Design and implement technical solutions that produce submission-ready outputs for regulators.
• Lead and support electronic submissions for significant regulatory filings.

Skills

Statistical programming

SAS

CDISC/SDTM/ADaM

Education

Degree in Statistics/Biostatistics/Mathematics/Computer Science/Life Sciences

Tools

SAS

CDISC/SDTM/ADaM

Job description

Bristol Myers Squibb is seeking a Principal Statistical Programmer in Uxbridge to join our GBDS team. You will transform complex clinical data into submission-ready outputs, working with cross-functional teams to influence regulatory decisions and patient outcomes.

You will design technical solutions using SAS and CDISC standards, contribute to SAS programming strategies, and participate in end-to-end data pipelines for major trials in a hybrid UK setting.