Senior Statistician - Remote, Global Trials & Growth

Warman O'Brien; United Kingdom; Remote; GBP 60,000 - 90,000; Full time

Benefits offered by this job

Fully remote UK

Competitive salary and bonus

Comprehensive benefits

International trials exposure

Training and mentoring

Career progression

Supportive global CRO environment

Job summary

Global CRO is seeking Senior Statistician roles at Senior I/II level to support UK and European expansion. The position offers ownership of clinical studies, close client collaboration, and structured training and career progression within a growing global CRO.

You will contribute to trial design, SAPs and study reports, perform analyses, support regulatory submissions, and lead cross-functional study delivery.

Qualifications

• MSc in Statistics, Biostatistics or related discipline.
• 4+ years' clinical trial statistics experience in CRO/pharma.
• Advanced SAS programming skills.
• Strong knowledge of statistical methodologies and trial design.
• Experience developing SAPs and supporting study reports.
• Excellent communication, organisational and problem-solving skills.

Responsibilities

• Provide statistical input into trial design, analysis and reporting.
• Develop and review protocols, SAPs and clinical study reports.
• Perform statistical analyses and review TLFs.
• Support regulatory submissions and ensure compliance with industry standards.
• Collaborate with clients and cross-functional teams.
• Take increasing responsibility for study delivery and statistical leadership.

Skills

Advanced SAS programming

Statistical methodologies

Communication skills

Problem solving

Organisational skills

Education

MSc in Statistics/Biostatistics

Tools

SAS

Job description

Global CRO is seeking Senior Statistician roles at Senior I/II level to support UK and European expansion. The position offers ownership of clinical studies, close client collaboration, and structured training and career progression within a growing global CRO.

You will contribute to trial design, SAPs and study reports, perform analyses, support regulatory submissions, and lead cross-functional study delivery.