Senior Biostatistician, Regulated Medical Devices

BD; Oklahoma; On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical benefits

Retirement plan

Paid time off

Educational assistance

Job summary

BD is seeking a Statistician/Biostatistician to support product development, clinical studies, and business decisions in a regulated healthcare environment. The role collaborates with cross-functional teams to design studies, develop analysis plans, and communicate insights.

Master’s or PhD in statistics/biostatistics with R/SAS programming is desired. Ideal candidates will manage multiple projects, ensure regulatory compliance, and contribute to scientific communications.

Qualifications

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

Responsibilities

• Design studies and plan analyses to support product development and clinical studies.
• Analyze complex data sets and communicate actionable insights to stakeholders.
• Program, document, validate, and maintain statistical analyses in R/SAS.
• Present findings to cross-functional teams and support regulatory submissions.

Skills

Statistical analysis

R programming

SAS programming

Study design

Regulatory knowledge

Cross-functional collaboration

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 in a regulated healthcare environment. The role collaborates with cross-functional teams to design studies, develop analysis plans, and communicate insights.

Master’s or PhD in statistics/biostatistics with R/SAS programming is desired. Ideal candidates will manage multiple projects, ensure regulatory compliance, and contribute to scientific communications.