Senior Statistical Programmer - Global Leading CRO - Home Based

Warman O’Brien; United Kingdom; Remote; GBP 45,000 - 65,000; Full time

Job summary

A leading CRO is seeking Senior Statistical Programmers to join their growing team remotely in the UK. This role involves leading programming projects, ensuring high-quality deliverables, and compliance with clinical data standards. With a focus on work-life balance and a generous remuneration package, this is an excellent opportunity for experienced professionals in the field.

Benefits

Flexible hours

Healthy work-life balance

Generous remuneration package

Qualifications

• 6 years’ experience in statistical programming.
• Excellent knowledge of SAS essential.
• 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 and ensure CDISC compliance.

Skills

SAS

R

CDISC

SDTM

ADaM

Education

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

Bachelor’s degree in Statistics, Biostatistics or Computer Sciences

Job description

Senior 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 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.
• 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 [phone] for a confidential discussion about potential opportunities.