Biostatistician - Contract

Posted 2026-05-05
Remote, USA Full-time Immediate Start

Biostatistician – (Contract)

The Biostatistician will perform statistical duties for one or more particular life science client projects, including clinical trial studies within the in-vitro diagnostic (IVD), medical device and pharmaceutical industry.

Beaufort is a global CRO built around one purpose- helping life science companies improve and save lives through rapid development and commercialization of innovative products.

    Key responsibilities include:
  • Conduct project planning activities such as:

o Protocol and Case Report Form (CRF) Review

o Sample size calculations

o Statistical Analysis Plan (SAP)

    o Programming Plan (including analysis dataset specifications)
  • Review project datasets and perform statistical analysis according to the plan (SAP).
  • Incorporate client changes or modifications as required and provide documentation logs to include in the project/study files.
  • Finalizes statistical analysis and final report for inclusion in the Clinical Study Report (CSR) and all appropriate project documentation. This includes tables, listings, and figures. Archive all documentation.
  • Perform other project-related tasks assigned to the Statistician role as specified in the individual’s Statement of Work.
    Qualifications:
  • Minimum of Master’s degree in statistics or biostatistics
  • 5+ years of experience
    Top 3 skills needed to perform the work requested:
  • Statistics, SAS programming skills, Knowledge of industry standards, Understanding of clinical trial data, preferably clinical trial data for in-vitro diagnostic trials
    Non-technical/ personal skills needed:
  • Effective communication both verbally and written, team player

Beaufort offers a different CRO experience. It’s not just about what we do, it’s how we do it. Together our team brings a level of passion, knowledge and commitment to our projects and clients. We foster a culture of excellence specializing in in-vitro diagnostics, clinical project management, quality oversight and regulatory solutions.

At Beaufort you will be part of industry leading expertise with a shared sense of purpose and unwavering accountability to help clients achieve successful market authorization.

Beaufort is an equal opportunity employer and values diversity.

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