Senior Biostatistician, Medical Devices & Trials

BD

Bozeman (MT)

On-site

USD 110,000 - 176,000

Full time

6 days ago
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Job summary

BD is seeking a Statistician/Biostatistician to support product development, clinical studies, and business decisions in a regulated healthcare environment. The role involves designing studies, developing analysis plans, and communicating insights to cross-functional teams.

The ideal candidate has a Master’s in Statistics or Biostatistics with 3+ years of experience and proficiency in R and/or SAS. You will design protocols, craft analyses, and help ensure regulatory compliance across projects.

Qualifications

  • Master's degree in Statistics, Biostatistics, or a related quantitative field.
  • 3+ years of experience in regulated healthcare, life sciences, or medical device environments.
  • Proficiency in programming, documenting, and validating analyses using R and/or SAS.

Responsibilities

  • Design, plan, and interpret studies and experiments supporting product development and business decisions.
  • Develop and review study protocols, CRFs, and regulatory documentation.
  • Program, document, and validate statistical analyses in R and/or SAS for data management and reporting.
  • Prepare clear, scientifically rigorous statistical reports for internal and external audiences.
  • Present findings to cross-functional stakeholders and contribute to publications and conferences.

Skills

Statistical analysis
R
SAS
Cross-functional teamwork
Regulatory knowledge

Education

Master's in Statistics/Biostatistics
PhD in Statistics/Biostatistics (preferred)

Tools

R
SAS

Job description

BD is seeking a Statistician/Biostatistician to support product development, clinical studies, and business decisions in a regulated healthcare environment. The role involves designing studies, developing analysis plans, and communicating insights to cross-functional teams.

The ideal candidate has a Master’s in Statistics or Biostatistics with 3+ years of experience and proficiency in R and/or SAS. You will design protocols, craft analyses, and help ensure regulatory compliance across projects.

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