Senior Statistician

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

We are partnering with a highly respected global CRO looking to appoint several Senior Statisticians at Senior I and Senior II level as part of its continued UK and European expansion.

This is an excellent opportunity to take greater ownership of clinical studies, work closely with clients and benefit from structured training, mentoring and long-term career progression within a growing organisation.

What you will be doing:

• Providing statistical input into clinical trial design, analysis and reporting.
• Developing and reviewing protocols, Statistical Analysis Plans (SAPs) and clinical study reports.
• Performing statistical analyses and reviewing TLFs.
• Supporting regulatory submissions and ensuring compliance with industry standards.
• Collaborating with clients and cross-functional teams.
• Taking increasing responsibility for study delivery and statistical leadership.

What you will need:

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

What's in it for you:

• Fully remote working anywhere in the UK.
• Competitive salary, bonus and comprehensive benefits.
• Exposure to varied international clinical trials.
• Excellent training, mentoring and long-term career progression.
• Supportive working environment within a growing global CRO.