Study Design Statistician – UK (Remote)

Role Overview

As part of our Strategic Statistical Services Arm, this is a full‑time role with emphasis on being an internal and external SME for clinical trial design, together with providing consultation to advise clients on a range of broader statistical issues, and will have an internal job title of Strategic Statistician.

Responsibilities

• Assist customers with their study design with a particular focus on simulation with KerusCloud to ensure they are aligned with the study objectives
• Preparation of study protocols and development of Statistical Analysis Plans and Statistical Analysis Reports
• Summarize, analyze and visualize study data using a variety of statistical methods, ultimately delivering results to an agreed timeline with optimal quality
• Provide statistical consultancy support to sponsors across the full span of clinical development, including oversight of third‑party statistical and programming deliverables
• Maintain current knowledge of relevant research techniques such as modelling, simulation and experimental design and participate in continuous professional development activity
• Support pre‑sales discussions to understand and identify client needs, then contribute to technical solutions and resource/cost estimates
• Collaborate with the Product Development team defining key features and statistical aspects of KerusCloud
• Provide input and support to marketing of KerusCloud, including demonstrations to clients and white papers

Requirements

• Bachelor’s degree in mathematics, statistics, physics, pharmacology or with a strong statistical component; Master’s or PhD preferred
• 5–7 years of experience in the application of medical statistics (pharma, CRO, academic)
• Willingness to engage with clients to understand and research problems and provide creative, business‑orientated solutions
• Experience in delivering customer projects to high‑quality standards
• Experience in SAS and/or R statistical software packages
• Experience in study design, protocol and report‑writing preferred
• Experience of modelling and simulation techniques to explore complex study designs preferred
• Experience of Bayesian approaches to design and analysis of clinical data preferred
• Experience of early‑phase drug development processes including innovative/adaptive study design preferred

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