Biostatistician III

Target PR Range: $75–85/hr depending on experience.

About the role

The Statistical Sciences Contractor will support the execution of the PULSEcheck (Progressive Uptake of Live Scientific Evaluation) initiative by partnering with study teams to monitor ongoing clinical trials and generate timely, data-driven insights. This role focuses on reviewing accumulating clinical-trial data, evaluating predefined PULSEcheck criteria, conducting exploratory analyses, and supporting informed decision-making throughout study execution. The contractor will work closely with study statisticians, programmers, and cross-functional stakeholders to assess study progress, identify emerging trends and risks, and provide analytical support that enhances trial oversight while maintaining scientific rigor.

Responsibilities

• Oversee all aspects of statistical planning and analyses for clinical programs.
• Direct both internal and external SAS programming efforts related to the responsible clinical programs.
• Prepare analysis programs for clinical trials (phases I–III).
• Serve as the primary statistician on at least one NDA/BLA.
• Conduct exploratory analyses, interim analyses, and data-monitoring activities.
• Translate complex datasets into actionable insights for cross-functional teams.

Requirements

• Master’s degree or PhD in Statistics, Biostatistics, Data Science, Mathematics, Epidemiology, or a related quantitative field.
• 5–7 years of experience in the pharmaceutical or biotechnology industry.
• Sound knowledge of statistical applications for clinical trials and drug-development regulations pertinent to trial design and statistical analysis.
• Strong knowledge of and experience in clinical-trial design.
• Excellent writing and communication skills.

Skills

• Statistical programming in R (SAS experience is a plus).
• Analyzing complex datasets.