Principal Statistical Programmer

Warman O'Brien; United Kingdom; Remote; GBP 60,000 - 80,000; Full time

Job summary

A leading CRO is seeking experienced Principal Statistical Programmers to join their dynamic team. The role offers the flexibility of remote work within the UK, focusing on high-quality deliverables and regulatory compliance in clinical research. Ideal candidates will have a strong background in statistical programming and a commitment to excellence in service delivery.

Benefits

Flexible hours promoting work-life balance

Fully remote work within the UK

Qualifications

• At least 8 years of experience in clinical trial statistical programming.
• Proficiency in SAS is essential; R knowledge is advantageous.

Responsibilities

• Lead statistical programming projects, ensuring high-quality, on-time deliverables.
• Develop and validate SDTM and ADaM datasets.
• Perform QC reviews and ensure CDISC compliance.

Skills

SAS

R

CDISC

SDTM

ADaM

Education

Bachelor’s degree in Statistics

Master’s or Ph.D.

Job description

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 the pharmaceutical, biotechnology, and medical device industries worldwide.

Renowned for high-quality deliverables, exceptional customer service, and flexibility, this organization offers a dynamic, entrepreneurial culture with ongoing growth and exciting career opportunities.

We are seeking experienced Principal Statistical Programmers to join remotely from anywhere in the UK.

Responsibilities:

• Lead statistical programming projects, ensuring high-quality, on-time deliverables.
• Develop and validate SDTM and ADaM datasets.
• Perform QC reviews and ensure CDISC compliance.
• Resolve Pinnacle 21 validation issues and review TLFs for consistency.
• Contribute to regulatory submissions, create define.xml files, develop macros, and perform data integrity checks.
• Maintain proper documentation and ensure SOP compliance.

Requirements:

• Bachelor’s degree in Statistics, Biostatistics, or Computer Sciences; Master’s or Ph.D. preferred.
• At least 8 years of experience in clinical trial statistical programming.
• Proficiency in SAS is essential; R knowledge is advantageous.
• Good understanding of data structures such as CDISC, SDTM, and ADaM.
• Knowledge of clinical data standards, TLFs, and submission guidelines.

What We Offer:

• Involvement in a growing organization.
• Flexible hours promoting work-life balance.
• Fully remote work within the UK.

Next Steps:

• If interested, please apply now with your CV. We are looking to arrange interviews promptly.

Contact:

• For confidential discussions, contact Jo Fornaciari at [phone].

Additional Information:

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Analyst, Science, and Information Technology
• Industries: Pharmaceutical Manufacturing and Biotechnology Research