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Senior Statistical Programmer

Warman O'BrienUnited Kingdom🇬🇧United KingdomPosted 2 Aug 2026

Why This Role Stands Out

Advance your career as a Senior Statistical Programmer within a leading, rapidly growing CRO, where you'll contribute to impactful clinical research projects from a remote UK location. This role is perfect for experienced statistical programmers who excel in SAS and CDISC standards, offering excellent growth potential and the chance to join a dynamic, entrepreneurial team. Apply now to leverage your expertise and drive your professional development in a flexible, supportive environment.

Quick Overview

Seniority
Mid Senior
Work mode
Remote
Location
United Kingdom
Clinical ResearchCompliance

Job Description

Senior Statistical Programmer I / II | Leading CRO | Home Based | UK | Permanent |


Join a fast-growing, independent CRO providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries.


Renowned for its high-quality deliverables, exceptional customer service, and flexibility in meeting clients’ needs this growing organisation offers a flexible, dynamic, and entrepreneurial culture. With ongoing growth and exciting career opportunities, it’s the perfect place to advance your career.


We’re seeking several Senior Statistical Programmers to join this growing organisation remotely from anywhere in the UK.


What you will be doing:

  • You’ll lead statistical programming projects, ensuring high-quality, on-time deliverables.
  • This includes developing and validating SDTM and ADaM datasets, performing QC reviews, and ensuring CDISC compliance.
  • You’ll resolve Pinnacle 21 validation issues, review TLFs for consistency, and contribute to regulatory submissions.
  • You'll also create define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs.


What you will need:

  • A Master’s or Ph.D. degree in Statistics, Biostatistics or Computer Sciences.
  • At least 6 years’ experience in clinical trial Statistical Programming.
  • Excellent knowledge of SAS essential with R advantageous.
  • Good working knowledge of data structures e.g. CDISC, SDTM, ADaM,
  • Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines.


What in it for you:

  • The opportunity to be involved in a growing organisation.
  • Focus on career development and progression.
  • Enjoy a healthy work-life balance with flexible hours that fit your lifestyle.
  • Fully remote in the UK
  • Generous remuneration package.


What to do next:

If this opportunity is of interest, please apply now with your CV as the organisation are looking to arrange interviews for the Senior Statistical Programmer as soon as possible.


Not what you’re looking for?

Please contact Jo Fornaciari on for a confidential discussion about potential opportunities.


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