Senior Biostatistician - MedTech Clinical Analytics

BD; Kansas City (MO); On-site; USD 110,000 - 176,000; Full time

Job summary

BD is seeking a Statistician/Biostatistician to support product development, clinical studies, and business decisions within a regulated healthcare environment. The role will collaborate with cross-functional teams to design studies, develop analysis plans, and communicate insights using R or SAS.

The successful candidate will apply advanced methods, program analyses, and prepare technical reports to ensure regulatory and quality objectives are met.

Qualifications

• Master's degree in Statistics, Biostatistics, or related quantitative field.
• 3+ years of experience in regulated healthcare, life sciences, or medical device environment.
• Experience applying statistical methods to product development, clinical research, or clinical trials.
• Proficiency in R and/or SAS for programming, documenting, and validating analyses.
• Experience leading cross-functional teams and managing multiple projects.

Responsibilities

• Design, plan, and interpret studies to support product development and business decisions.
• Develop and review study protocols, CRFs, and regulatory documents.
• Develop and maintain statistical analysis plans; consult for complex issues.
• Program, document, validate, and maintain statistical code in R/SAS.
• Prepare clear statistical reports and technical documentation for internal/external audiences.
• Present findings to stakeholders and contribute to publications or conferences.

Skills

Statistical analysis

Regulatory compliance

Cross-functional collaboration

R programming

SAS programming

Data analysis

Report writing

Education

Master's degree in Statistics/Biostatistics

3+ years in regulated healthcare/medical device

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. The role will collaborate with cross-functional teams to design studies, develop analysis plans, and communicate insights using R or SAS.

The successful candidate will apply advanced methods, program analyses, and prepare technical reports to ensure regulatory and quality objectives are met.