Principal Statistician - Early Phase

📋 Description

• Senior statistical expert supporting clinical studies across all phases of development, from
• Provide statistical leadership on studies, including design, analysis, randomization, and
• Develop and oversee Statistical Analysis Plans (SAPs) with specifications, tables, listings, and
• Support creation/review of analysis datasets, programming specs, and trial documentation.
• Collaborate with clinical, data management, programming, regulatory, and project management teams
• Conduct QC reviews of statistical deliverables for accuracy and standards compliance.

🎯 Requirements

• Graduate degree in Biostatistics, Statistics, Mathematics, or related quantitative field.
• Extensive experience in clinical trials/biostatistics with ability to lead complex projects.
• Strong understanding of statistical methods, trial design, analysis techniques, and ICH guidelines.
• Experience across complete statistical lifecycle: protocol, SAP, analysis, CSR.
• Proficiency in R programming for clinical research.
• Regulatory submission experience desirable.

🎁 Benefits

• Fully remote opportunity from Europe with flexible work arrangements.
• Opportunity to contribute to meaningful clinical research programs supporting new therapies.
• Collaboration with international scientific and healthcare teams.
• Career development through training, mentorship, and exposure to diverse therapeutic areas.
• Access to a global environment focused on innovation and knowledge sharing.
• Experience across complex clinical studies and stages of drug development.