Senior Biostatistician — MedTech Clinical Analytics

BD; Austin (TX); On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

Medical benefits

Retirement plan

Paid time off

Educational assistance

Job summary

BD seeks a Statistician/Biostatistician to support product development, clinical studies, and regulatory decisions in a healthcare setting. The role involves study design, analysis planning, and delivering actionable insights across cross-functional teams.

The candidate should hold a Master’s or PhD in Statistics/Biostatistics with experience in regulated healthcare or medical devices, and be proficient in R or SAS.

Qualifications

• Master's degree in Statistics, Biostatistics, or related field.
• 3+ years of experience in regulated healthcare, life sciences, or medical device environment.
• Proficiency in R and/or SAS for analyses.
• Experience designing studies and clinical trials.
• Ability to manage multiple projects in a fast-paced environment.
• PhD in Statistics/Biostatistics or related field.
• Experience applying statistical methodologies in manufacturing, quality, or regulatory initiatives.
• Knowledge of reproducible research environments.

Responsibilities

• Design studies and analysis plans for product development and clinical studies.
• Analyze complex data sets and communicate actionable insights.
• Program, validate, and maintain statistical code in R and/or SAS.
• Prepare technical reports and regulatory documentation.
• Present findings to stakeholders and contribute to publications.
• Collaborate with cross-functional teams to support regulatory decisions.

Skills

Statistical methods

R programming

SAS programming

Project management

Regulatory awareness

Data interpretation

Education

Master's degree in Statistics/Biostatistics

PhD in Statistics/Biostatistics

Equivalent education/experience

Tools

R

SAS

Job description

BD seeks a Statistician/Biostatistician to support product development, clinical studies, and regulatory decisions in a healthcare setting. The role involves study design, analysis planning, and delivering actionable insights across cross-functional teams.

The candidate should hold a Master’s or PhD in Statistics/Biostatistics with experience in regulated healthcare or medical devices, and be proficient in R or SAS.