Senior Biostatistician — SAS, CDISC & Regulatory

Worldwide Clinical Trials; Nottingham; On-site; GBP 60,000 - 95,000; Full time

Job summary

Worldwide Clinical Trials in the United Kingdom is seeking an experienced statistician to join our Biostatistics team. You will contribute to study design, analysis plans, and reporting across therapeutic areas, ensuring high-quality statistical deliverables.

You will work with sponsors, data managers and statisticians, develop SAS programs, and help interpret results for regulatory submissions. A strong track record in clinical statistics and English communication is essential.

Qualifications

• Appropriate degree and minimum relevant experience: BSc/8 years, MSc/6 years, PhD/4 years.
• Hands-on expert level project statistician with statistical leadership.
• Broad experience across statistical applications and regulatory standards.

Responsibilities

• Review study designs, analysis plans, and reports; contribute to trial design and SPA writing.
• Develop, test, and run SAS programs for statistical analysis of study data.
• Prepare final reports with tables, figures, and listings; support reporting.
• Identify system and process improvements to enhance data processing quality.
• Provide statistics support to projects, ensuring timely consultancy and delivery.

Skills

SAS

Analytical thinking

Communication

Education

BSc

MSc

PhD

Tools

SAS

Job description

Worldwide Clinical Trials in the United Kingdom is seeking an experienced statistician to join our Biostatistics team. You will contribute to study design, analysis plans, and reporting across therapeutic areas, ensuring high-quality statistical deliverables.

You will work with sponsors, data managers and statisticians, develop SAS programs, and help interpret results for regulatory submissions. A strong track record in clinical statistics and English communication is essential.