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Senior Statistical Programmer

Warman O'Brien

United Kingdom

Remote

GBP 50,000 - 70,000

Full time

2 days ago

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Job summary

A leading independent CRO is seeking a Senior Statistical Programmer to join their remote team in the UK. The role involves leading statistical programming projects, ensuring high-quality deliverables, and maintaining compliance with industry standards. Ideal candidates will have a strong background in statistics and programming, with a focus on clinical trial data.

Benefits

Flexible hours

Healthy work-life balance

Qualifications

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.

Responsibilities

Lead statistical programming projects, ensuring high-quality deliverables.
Develop and validate SDTM and ADaM datasets, perform QC reviews.
Ensure compliance with CDISC standards and create define.xml files.

Skills

SAS

CDISC

Statistical Programming

Education

Bachelor’s degree in Statistics, Biostatistics or Computer Sciences

Masters or Ph.D. in Statistics

1 week ago Be among the first 25 applicants

Senior Statistical Programmer | Independent 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 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 Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics.
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.
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 Statistical Programmers as soon as possible.

Not what you’re looking for?

Please contact Jo Fornaciari on +44 7488 822 859 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 Research
Industries
Pharmaceutical Manufacturing and Biotechnology Research

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