Senior Biostatistician: Study Design & Analysis Lead

Worldwide; United Kingdom; Remote; GBP 70,000 - 95,000; Full time

Job summary

Worldwide Clinical Trials is seeking an experienced biostatistician in the United Kingdom to join the Biostatistics and Statistical Programming team. You will review study designs, contribute to trials, and lead statistical analyses across multiple sponsors and therapeutic areas.

The role emphasizes SAS programming, regulatory compliance and collaboration with cross‑functional teams to deliver high‑quality results.

Qualifications

• Advanced degree in statistics or biostatistics with clinical trial exposure.
• Strong SAS programming and data handling skills.
• Knowledge of CDISC standards and regulatory expectations.

Responsibilities

• Review study designs, analysis plans and reports.
• Contribute to design of clinical trials, SAPl, randomization methodology.
• Provide statistical leadership across projects and sponsor programs.
• Develop SAS programs for analysis of clinical study data and derived datasets.
• Prepare final reports with tables, figures and listings.
• Ensure compliance with ICH, FDA and quality standards.
• Collaborate with sponsors, data managers and statisticians.

Skills

SAS

CDISC

Statistics

Study design

Regulatory knowledge

Communication

English proficiency

Education

Bachelor/Master/PhD in statistics or biostatistics

Tools

SAS software

Job description

Worldwide Clinical Trials is seeking an experienced biostatistician in the United Kingdom to join the Biostatistics and Statistical Programming team. You will review study designs, contribute to trials, and lead statistical analyses across multiple sponsors and therapeutic areas.

The role emphasizes SAS programming, regulatory compliance and collaboration with cross‑functional teams to deliver high‑quality results.