Senior Biostatistician – Medical Devices & Clinical Research

BD; Atlanta (GA); Vor Ort; USD 100.000 - 150.000; Vollzeit

Benefits dieser Stelle

Health insurance

401(k)

Paid time off

Parental leave

Zusammenfassung

BD is seeking a Statistician/Biostatistician to support product development, clinical studies, and business decisions in a regulated healthcare environment. You will design studies, develop analysis plans, and communicate insights using R or SAS.

The role requires a Master’s or PhD in Statistics/Biostatistics with 3+ years in regulated settings, strong programming, and ability to influence stakeholders without direct authority. Familiarity with regulatory requirements is highly desirable.

Qualifikationen

• Master's or PhD in Statistics, Biostatistics, or related field.
• 3+ years of experience in regulated healthcare or medical device environment.
• Strong expertise in study design, statistical analysis, and data interpretation.
• Hands-on programming in R and/or SAS.
• Ability to manage multiple projects and influence stakeholders without direct authority.

Aufgaben

• Design, plan, analyze, and interpret studies and experiments supporting product development.
• Develop and review study protocols and regulatory documentation.
• Develop and maintain statistical analysis plans using R/SAS; validate analyses.
• Produce clear statistical reports for internal and external audiences.
• Present findings to cross-functional teams and contribute to publications or presentations.

Kenntnisse

Statistical analysis

R programming

SAS programming

Study design

Regulatory knowledge

Cross-functional collaboration

Data interpretation

Technical reporting

Regulatory submissions

Stakeholder management

Ausbildung

Master's in Statistics/Biostatistics

PhD in Statistics/Biostatistics

Tools

R

SAS

Jobbeschreibung

BD is seeking a Statistician/Biostatistician to support product development, clinical studies, and business decisions in a regulated healthcare environment. You will design studies, develop analysis plans, and communicate insights using R or SAS.

The role requires a Master’s or PhD in Statistics/Biostatistics with 3+ years in regulated settings, strong programming, and ability to influence stakeholders without direct authority. Familiarity with regulatory requirements is highly desirable.