Offer summary

Qualifications:

Minimum of Master’s degree in statistics or biostatistics, 5+ years of experience in the field, Proficiency in SAS programming and statistical analysis, Strong understanding of clinical trial data, especially for in-vitro diagnostics..

Key responsabilities:

Conduct project planning activities including protocol and CRF review

Perform statistical analysis according to the Statistical Analysis Plan (SAP)

Finalize statistical analysis and prepare reports for Clinical Study Reports (CSR)

Incorporate client changes and maintain documentation logs for project files.

Job description

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.

Required profile