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Principal Statistical Programmer

Warman O'Brien

United Kingdom

Remote

GBP 45,000 - 75,000

Full time

10 days ago

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Job summary

Join a dynamic and growing independent CRO as a Principal Statistical Programmer. This role offers the chance to lead statistical programming projects while ensuring high-quality deliverables in a fully remote environment. You will have the opportunity to work with cutting-edge clinical research services, developing and validating datasets, and contributing to regulatory submissions. With a focus on flexibility and work-life balance, this position is perfect for those looking to advance their careers in a supportive and entrepreneurial culture. Don't miss out on this exciting opportunity to make a significant impact in the industry!

Benefits

Flexible working hours

Healthy work-life balance

Remote work opportunity

Qualifications

6 years’ experience in statistical programming required.
Excellent knowledge of SAS essential with R advantageous.

Responsibilities

Lead statistical programming projects ensuring high-quality deliverables.
Develop and validate SDTM and ADaM datasets, perform QC reviews.

Skills

SAS

CDISC

SDTM

ADaM

Education

Master’s or Ph.D. in Statistics, Biostatistics, or Computer Sciences

Bachelor’s degree in Statistics, Biostatistics, or Computer Sciences

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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 several Senior & 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 Master’s or Ph.D. degree in Statistics, Biostatistics or Computer Sciences and 6 years’ experience in statistical programming.
OR A Bachelor’s degree in the above fields with 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.
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 Information Technology
Industries
Pharmaceutical Manufacturing and Biotechnology Research

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