Lead Statistical Programmer – Regulatory Submissions

Biopharma Careers

Uxbridge

Hybrid

GBP 70,000 - 95,000

Full time

10 days ago

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Benefits offered by this job

50% Hybrid Working

Job summary

Bristol Myers Squibb is seeking a Principal Statistical Programmer to join the Global Biometrics & Data Sciences (GBDS) team in a flexible hybrid role based in Uxbridge. You will be embedded with cross-functional teams to turning complex clinical data into submission-ready outputs for regulators, using SAS and CDISC standards to shape regulatory submissions and patient outcomes.

With 7+ years in pharma statistical programming, you will influence strategy, mentor others, and lead electronic

Qualifications

7+ years of statistical programming experience in the pharmaceutical/biopharma industry.
Fluent in SAS and CDISC/SDTM/ADaM standards and end-to-end data pipelines.
Experience designing and delivering submissions-ready outputs for regulators.

Responsibilities

Embedded in cross-functional teams with statisticians, data managers, and scientists.
Turn complex clinical data into submission-ready outputs that regulators can trust.
Design and implement technical solutions that influence regulatory outcomes and patient impact.
Lead or support electronic submissions for significant regulatory filings.