Principal Statistical Programmer

Warman O'Brien; United Kingdom; Remote; GBP 50,000 - 70,000; Full time

Job summary

A leading Clinical Research Organization is seeking a Principal Statistical Programmer to join their team remotely in the UK. The role involves overseeing statistical programming projects and ensuring compliance with industry standards while working in a flexible and dynamic environment. Candidates should have extensive programming experience and a strong educational background in Statistics.

Benefits

Flexible work hours

Healthy work-life balance

Fully remote position

Qualifications

• 8 years experience in clinical trial statistical programming required.
• Excellent knowledge of SAS essential with R advantageous.
• Good working knowledge of data structures e.g. CDISC, SDTM, ADaM.

Responsibilities

• Lead statistical programming projects ensuring high-quality deliverables.
• Develop and validate SDTM and ADaM datasets, perform QC reviews.
• Resolve validation issues and contribute to regulatory submissions.

Skills

SAS

R

CDISC

data integrity

Education

Bachelor's degree in Statistics or Biostatistics

Masters or Ph.D. in Statistics

Job description

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Principal Statistical Programmer | Leading CRO | Home Based | UK |

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 elite Principal 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 Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics.
• 8 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.
• Enjoy a healthy work-life balance with flexible hours that fit your lifestyle.
• Fully remote in the UK

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 Principal Statistical Programmers as soon as possible.

Not what you’re looking for?

• Please contact Jo Fornaciari on [phone] for a confidential discussion about potential opportunities.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Analyst, Science, and Information Technology

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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