Senior Biostatistician - MedTech Clinical Studies Lead

BD; Louisiana; Presencial; USD 110.000 - 150.000; Jornada completa

Descripción de la vacante

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

The ideal candidate holds a Master’s or PhD in Statistics or Biostatistics, with hands-on R/SAS programming and experience in regulated healthcare or medical device settings.

Formación

• Master's or PhD in Statistics, Biostatistics, or related quantitative 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 experience in R and/or SAS
• Ability to manage multiple projects and influence stakeholders in cross-functional teams
• Experience with regulatory requirements and quality/regulatory environments

Responsabilidades

• Design studies and create statistical analysis plans for product development and clinical studies
• Analyze complex data sets and communicate actionable insights
• Program, document, validate, and maintain statistical code in R and/or SAS
• Deliver high-quality analyses supporting project milestones across products and platforms
• Present findings to cross-functional stakeholders and contribute to publications or external communications
• Stay current with emerging statistical methods and regulatory requirements

Conocimientos

Statistical analysis

Study design

Regulatory knowledge

Data interpretation

Cross-functional collaboration

Educación

Master's degree in Statistics or Biostatistics

PhD in Statistics / Biostatistics

Herramientas

R

SAS

Programming & reproducible research

Descripción del empleo

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

The ideal candidate holds a Master’s or PhD in Statistics or Biostatistics, with hands-on R/SAS programming and experience in regulated healthcare or medical device settings.