Principal Statistician for Clinical Studies - Remote

Overview

The Principal Statistician is responsible for leading statistical deliverables for clinical studies, providing expertise in research design, analysis, and reporting.

In Short

• Lead statistician on clinical studies.
• Provide statistical expertise for trial design and analysis.
• Collaborate with project teams and external experts.
• Prepare clinical study reports and regulatory documents.
• Drive submission activities and responses to regulatory authorities.
• Use SAS and R for statistical analysis and reporting.
• Ensure compliance with quality management systems.
• Identify opportunities for productivity improvements.
• Communicate statistical concepts to non-statisticians.
• Remain current with statistical methods and trial design issues.

Requirements

• Masters’ degree in Statistics, Biostatistics, or related field.
• 5+ years of experience in clinical trial analysis.
• Working knowledge of SAS and R required.
• Experience with FDA regulatory requirements preferred.
• Strong organizational skills and attention to detail.
• Excellent communication skills.

Benefits

• Competitive compensation package.
• Benefits and equity program when applicable.
• Opportunities for professional development.