Principal Statistician - Early Phase

Tasks

• Create statistical analysis plans
• Define statistical programming specifications
• Develop analysis strategies
• Lead clinical study statistical design
• Manage protocol through CSR statistical lifecycle
• Mentor biostatistics colleagues
• Oversee SAP mockup tables listings figures
• Perform statistical quality control reviews
• Provide interpretation of clinical trial results
• Review analysis datasets
• Support DSMB DMC statistical input review
• Support regulatory submissions

Perks/Benefits

• Flexible work arrangements
• Fully remote from Europe
• Global collaboration
• Inclusive workplace culture
• Mentorship
• Professional development opportunities
• Training

Skills/Tech-stack

Analysis Plan | Biostatistics | Clinical Trial Design | Clinical data | Clinical trial | Data Monitoring | Data Monitoring Committee | Data Safety | Data safety monitoring | Dataset development | ICH | Quality Control | R | Randomization | Regulatory guidelines | Safety monitoring | Statistical Analysis | Statistical Analysis Plan | Statistical programming | Trial design