Senior Biostatistician, Regulated MedTech Analytics

BD

Clayton (MO)

On-site

USD 110,000 - 165,000

Full time

6 days ago
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Benefits offered by this job

Medical, dental, vision
Life and disability insurance
401(k) retirement plan
Paid time off and holidays
Parental leave
Educational assistance

Job summary

BD is seeking a Statistician/Biostatistician to support product development, clinical studies, and business decisions within a regulated healthcare environment. You will design studies, develop analysis plans, analyze complex data, and communicate insights to cross-functional teams.

The role requires a Master's or PhD in Statistics or Biostatistics, strong skills in R and/or SAS, experience with regulatory requirements, and the ability to manage multiple projects in a fast-paced medical device

Qualifications

  • Master's or PhD in Statistics, Biostatistics, or a related field.
  • Experience supporting clinical research, product development, or regulated healthcare environments.
  • Strong study design, statistical analysis, and data interpretation skills.
  • Hands-on programming in R and/or SAS; reproducible research practices.

Responsibilities

  • Design, plan, and analyze studies to support product development and regulatory needs.
  • Develop statistical analysis plans and validate analyses in R and/or SAS.
  • Communicate actionable insights to cross-functional stakeholders and leadership.
  • Ensure analyses meet quality, regulatory, and business objectives.

Skills

Study design
Statistical analysis
Data interpretation
R programming
SAS programming
Regulatory knowledge
Reproducible research

Education

Master's in Statistics/Biostatistics
PhD in Statistics/Biostatistics

Tools

R
SAS

Job description

BD is seeking a Statistician/Biostatistician to support product development, clinical studies, and business decisions within a regulated healthcare environment. You will design studies, develop analysis plans, analyze complex data, and communicate insights to cross-functional teams.

The role requires a Master's or PhD in Statistics or Biostatistics, strong skills in R and/or SAS, experience with regulatory requirements, and the ability to manage multiple projects in a fast-paced medical device

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