Principal Statistician - Early Phase

📋 Description

• Senior statistical expert for clinical studies across development stages.
• Lead study design, analysis strategies, and interpretation of results.
• Develop and review SAPs with mock-up tables/listings/figures.
• Support data sets, programming specs, and trial documentation.
• Collaborate with clinical, data management, regulatory, and PM teams.
• QC statistical deliverables for accuracy and standards.

🎯 Requirements

• Graduate degree in Biostatistics/Statistics/Math or related field.
• Extensive experience in clinical trials/biostatistics; lead complex projects.
• Strong understanding of statistical methods, trial design, and ICH guidelines.
• Experience across protocol, SAP, analysis, and CSR lifecycle.
• Proficient in R; experience with clinical research programming.
• Regulatory submission experience is desirable.

🎁 Benefits

• Fully remote opportunity from Europe with flexible arrangements.
• Impact meaningful clinical research programs.
• Collaborate with international scientific teams.
• Career development through training and mentorship.
• Global environment focused on innovation and growth.
• Work on complex studies across drug development stages.