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Statistician

Alimentiv
5 hours ago
Full-time
On-site
London, 08

JobsCloseBy Editorial Insights

Alimentiv is hiring multiple Statisticians to apply biostatistical methods across clinical trials and data management, covering planning, design, analysis and reporting throughout the project life cycle in line with regulatory standards. You will act as a subject matter expert, supporting project teams, quality audits and external stakeholders, and contribute to Alimentiv’s global research footprint through data development, publication and reporting. Roles span Analysis Services, Academic Research Support, Project Support, Statistical Analysis and Data Collection Planning, and Study Report Support. Requirements include a bachelor’s or master’s degree plus 1-3 years of relevant experience and a professional designation. These full-time roles offer home-based options with possible London involvement. Tips: tailor your CV to show trial statistics, SAP work, regulatory familiarity, cross-functional collaboration, and concrete examples of analyses or publications; highlight software proficiency and the ability to translate statistics into biomedical insights.

Responsible for the application of biostatistical methods to support clinical trials and data management, including statistical planning, design, analysis, and reporting throughout the project life cycle in accordance with project, organizational and regulatory standards.  Act as subject matter expert, providing statistical support to project teams, quality/study auditors, and external stakeholders. Participate in the promotion of Alimentiv as a global research organization, by contributing to the development, publishing, and reporting of project data. Please note we are hiring for multiple positions at this time.

Analysis Services

  • Carry out statistical analyses and provide direction to programmers, using standard software packages to interpret and translate results within a statistical framework into biomedical terms and prepare statistical data results for inclusion in reports and research papers that meet trial, organizational and regulatory best practices, and standards.

Academic Research Support

  • Working in conjunction with the Director of Academic Research, convert and present new and novel biometrical trial technologies, processes and findings into publishable and promotable scientific processes and results.

Project Support

  • Provide statistical expertise and guidance based on established methodologies throughout the project life cycle in the areas of study policies, protocols, implementation timelines and processes, data interpretation and publication of results.
  • Work with data management team to ensure data captured incorporates and corresponds to project protocols and requirements.  

Statistical Analysis/Data Collection Planning

  • Prepare statistical analysis plan and oversee project data collection, management, and analysis with input from the project teams that incorporates the type of information collected, sample size, randomization procedures, table and listing shells, project statistical policies, protocols, and methodology to be used to appropriately translate scientific questions into statistical hypotheses.

Study Report Support

  • Assist medical director(s) and/or technical writers by preparing statistical section of study report, publications and/or presentations ensuring statistical analyses adheres to trial, sponsor, organizational and regulatory requirements, and best practices.

Qualifications

  • A minimum of a Bachelor's or Master's degree and a professional designation + 1-3 years of related experience.
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Working Conditions

  • Home-based.