Job Title: Senior Statistician I
Location: Witney, United Kingdom
Category: Medical & Clinical Affairs / Biostatistics
Industry: Medical Devices / Digital Health
Experience Required: 3–6 Years
Employment Type: Full-Time
The Senior Statistician I role is a key position within a Medical Devices Centre of Excellence in Witney, supporting the development of next-generation glucose monitoring technologies. This opportunity offers hands-on involvement across the full lifecycle of clinical trials, enabling direct contribution to innovative products that improve patient outcomes globally.
The role is ideally suited for experienced biostatistics professionals seeking exposure to global clinical projects, cross-functional collaboration, and leadership development within a high-growth medical technology environment.
Provide end-to-end statistical support for global clinical trials, typically spanning 4 to 18 months.
Contribute to protocol design, statistical analysis plans, interim analyses, and final clinical study reports.
Support the preparation of scientific publications and regulatory-ready statistical outputs.
Deliver statistical expertise for marketed and pipeline glucose monitoring products, including the FreeStyle Libre Flash Glucose Monitoring system.
Collaborate closely with scientists, engineers, and clinical teams to support data-driven product development.
Work within a collaborative, diverse, and high-performing statistics team across multiple projects and statistical methodologies.
Lead small project teams or workstreams, sharing best practices and driving continuous improvement.
Actively participate in internal statistical networks to enhance professional capability and consistency.
Demonstrate initiative by identifying opportunities to improve study design, analysis approaches, and data interpretation.
Communicate complex statistical concepts clearly to cross-functional stakeholders.
Balance priorities effectively while maintaining attention to detail in a fast-paced development environment.
Bachelor’s degree or higher in Statistics, Mathematics, or a related quantitative discipline
3 to 6 years of relevant experience in biostatistics or clinical research within medical devices, pharmaceuticals, or life sciences
Strong hands-on experience using SAS for clinical data analysis
Prior involvement in clinical trials and regulated research environments is essential
Advanced statistical analysis and data interpretation skills
Proficiency in SAS and clinical data standards
Strong written and verbal communication abilities
High attention to detail and quality
Ability to collaborate effectively within multidisciplinary teams
Demonstrated interest or initial experience in people or project leadership
Opportunity to work on cutting-edge glucose monitoring technologies with global patient impact
End-to-end exposure to clinical trials and product development
Structured career development and leadership pathways
Competitive compensation and comprehensive benefits package, including pension, healthcare, and flexible benefits
Work-life balance supported by a modern campus and wellbeing initiatives
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