Job Details
Senior Statistician
6187
Posted: 13/04/2026
- £Competitive
- Home Based - UK, United Kingdom
- Permanent
Senior Statistician | Global CRO | UK | Home Based | Permanent |
Due to expansion across Europe, we have a new opportunity for a Senior Statistician to join a growing Global CRO in the UK.
This organisation is recognised for its strong statistical expertise, high-quality delivery, and collaborative, client-focused approach. This is an excellent opportunity for an experienced statistician looking to take ownership of studies and progress towards leadership responsibilities.
What you will be doing:
What you will need:
What’s in it for you:
Due to expansion across Europe, we have a new opportunity for a Senior Statistician to join a growing Global CRO in the UK.
This organisation is recognised for its strong statistical expertise, high-quality delivery, and collaborative, client-focused approach. This is an excellent opportunity for an experienced statistician looking to take ownership of studies and progress towards leadership responsibilities.
What you will be doing:
- Support the delivery of clinical trial projects, providing statistical input across study design and analysis
- Contribute to protocol development, sample size calculations, and statistical analysis planning
- Perform statistical analyses and support interpretation of clinical data
- Write and review Statistical Analysis Plans (SAPs), statistical reports, and study documentation
- Collaborate with cross-functional teams including clinical, programming, and data management
- Review statistical outputs (tables, listings, figures) to ensure accuracy and quality Support regulatory submissions and ensure compliance with industry standards (e.g. CDISC)
- Contribute to process improvements and efficient study delivery
What you will need:
- Master’s degree in statistics, biostatistics, maths or computer sciences
- 4+ years’ experience in clinical trial statistics within a CRO or pharmaceutical environment
- Advanced level proficiency in SAS
- Solid understanding of clinical trial design and statistical methodologies
- Experience contributing to SAPs and clinical study reports
- Experience with Microsoft Word, Excel, PowerPoint, Outlook, Project
- Able to proactively initiate tasks and drive them to completion
- Strong attention to detail and problem-solving skills
- Able to manage multiple priorities and meet deadlines
- Builds strong working relationships with internal and external stakeholders
What’s in it for you:
- Work for a Global CRO and be part of continued expansion across Europe
- Competitive salary + bonus
- Eligible for medical, dental, vision, extended health benefits, pension, fitness subsidy & life insurance
- Fully home based in the UK
Jo Fornaciari
Principal Consultant in Statistical Programming
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