Consultant Statistician
Consultant Statistician
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1 Vacancy
Job Description
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This is a full-time remote position.
Job Description:
Our experienced statisticians and programmers develop intellectual property and assets to support the design and analysis of clinical trials precision medicine and real-world data analytics. We address the emerging analytics needs of the Industry with our biostatistics services bespoke algorithms and unique state of the art proprietary cloud-based trial simulation software KerusCloud. Working alongside innovative statisticians you will be responsible for leading the full life-cycle of KerusCloud support and statistical services from:
- Assisting 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.
- 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 white papers etc.
Requirements:
- Bachelors degree in mathematics statistics physics pharmacology or with a strong statistical component Masters 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 and 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.
Required Experience:
Senior IC
Employment Type
Full-Time
