Principal Statistician - Early Phase

📋 Description

• Serve as a senior statistical expert supporting clinical studies across all phases of development
• Provide statistical leadership on assigned projects, including study design, analysis strategies
• Develop, review, and oversee SAPs, including specifications and mock-up tables, listings, and
• Support the creation and review of analysis datasets, statistical programming specifications, and
• Partner with cross-functional teams including clinical, data management, programming, regulatory
• Conduct quality control reviews of statistical deliverables to ensure accuracy, consistency with

🎯 Requirements

• Graduate degree in Biostatistics, Statistics, Mathematics, or a related quantitative discipline.
• Extensive experience in clinical trials, biostatistics, or a comparable research environment, with
• Strong understanding of statistical methodology, clinical trial design, analysis techniques, and
• Experience supporting the complete statistical lifecycle of clinical studies, including protocol
• Proficiency in R programming and experience applying statistical programming techniques in clinical
• Experience reviewing or supporting regulatory submissions is highly desirable.

🎁 Benefits

• Fully remote working opportunity from Europe with flexible work arrangements.
• Opportunity to contribute to meaningful clinical research programs that support the development of
• Collaboration with international teams of scientific and healthcare experts.
• Career development opportunities through training, mentorship, and exposure to diverse therapeutic
• Access to a global environment focused on innovation, knowledge sharing, and professional growth.
• Opportunity to work on complex clinical studies and gain experience across different stages of drug