Senior Statistical Programmer — Hybrid Submissions

Bristol Myers Squibb; Denham; Hybrid; GBP 70,000 - 120,000; Full time

Job summary

Bristol Myers Squibb in the UK is seeking a Principal Statistical Programmer to join our Global Biometrics & Data Sciences team. You will transform complex clinical data into submission-ready outputs, ensuring accuracy and regulatory readiness.

You’ll work with CDISC standards, ADaM specifications, and SAS programming, collaborating with statisticians, data managers, and external vendors to influence the evidence package and patient outcomes.

Qualifications

• 7+ years of statistical programming in pharma/biopharma.
• Fluent with SAS, CDISC/SDTM/ADaM, and end-to-end clinical data pipelines.
• Knowledge of drug development lifecycle from eDC to e-submission.
• Ability to communicate with statisticians, clinicians, and regulators.
• Degree in Statistics, Biostatistics, Mathematics, CS or Life Sciences.

Responsibilities

• Lead and design technical solutions for clinical data and submissions.
• Work with CDISC standards, ADaM specs, SAS programming and electronic submissions.
• Embed in cross-functional teams with statisticians, data managers, and external vendors.
• Influence programming strategy and risk decisions at senior levels.
• Mentor and develop other technical professionals.

Skills

Statistical programming

SAS

CDISC/SDTM/ADaM

Regulatory submissions

Clinical data pipeline

Education

Statistics/Biostatistics/Mathematics/Computer Science/Life Sciences degree

Job description

Bristol Myers Squibb in the UK is seeking a Principal Statistical Programmer to join our Global Biometrics & Data Sciences team. You will transform complex clinical data into submission-ready outputs, ensuring accuracy and regulatory readiness.

You’ll work with CDISC standards, ADaM specifications, and SAS programming, collaborating with statisticians, data managers, and external vendors to influence the evidence package and patient outcomes.