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
#J-18808-Ljbffr