Senior SAS Programmer – Global Clinical Data Lead (Hybrid)

Bristol Myers Squibb

Denham

Hybrid

GBP 65,000 - 90,000

Full time

8 hours ago
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Job summary

Bristol Myers Squibb in Uxbridge, UK, is seeking a Senior Statistical Programmer in a hybrid role with 50% onsite work. You will lead SAS programming for derived analysis datasets, TFLs, and regulatory deliverables, while collaborating across the Global Biometrics & Data Sciences function.

The role emphasizes ownership of programming work, interaction with cross-functional clinical teams, and contribution to regulatory submissions and data standards as part of a world-class pharmacovigilance and

Qualifications

  • Bachelor’s degree in Statistics/Biostatistics/Math/CS/Life Sciences.
  • Industry experience in statistical programming.
  • Knowledge of SDTM/ADaM standards and clinical data structures.
  • Regulatory submission experience is advantageous.

Responsibilities

  • Write and validate SAS programs to generate derived analysis datasets and TFLs.
  • Support NDA, BLA, MAA submissions and regulatory milestones.
  • Review SAPs and Data Presentation Plans before programming work begins.
  • Collaborate with vendors on standards, specifications and file transfers.
  • Independently lead programming assignments across multiple projects with limited supervision.
  • Identify opportunities to improve GBDS efficiency and consistency.

Skills

SAS Proficiency
SDTM/ADaM
Data Handling
Regulatory Submissions

Education

Bachelor's degree in Statistics/Biostatistics/Math/CS/Life Sciences
Experience in statistical programming

Tools

MS Office
XML
Pinnacle 21
Linux

Job description

Bristol Myers Squibb in Uxbridge, UK, is seeking a Senior Statistical Programmer in a hybrid role with 50% onsite work. You will lead SAS programming for derived analysis datasets, TFLs, and regulatory deliverables, while collaborating across the Global Biometrics & Data Sciences function.

The role emphasizes ownership of programming work, interaction with cross-functional clinical teams, and contribution to regulatory submissions and data standards as part of a world-class pharmacovigilance and

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