Job Details
Biostatistician - Contract
2026-01-20 Beaufort all cities,AK
Description:
o Sample size calculations
o Statistical Analysis Plan (SAP)
o Programming Plan (including analysis dataset specifications)
Qualifications:
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.
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 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
- Statistics, SAS programming skills, Knowledge of industry standards, Understanding of clinical trial data, preferably clinical trial data for in-vitro diagnostic trials
- 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.