Principal Statistician - Early Phase

Tasks

• Collaborate with cross functional clinical teams
• Conduct quality control on statistical deliverables
• Create statistical analysis plans
• Design randomization approaches
• Develop analysis datasets specifications
• Develop protocol statistical strategy
• Interpret clinical trial results
• Lead complex integrated analyses
• Mentor biostatistics colleagues
• Provide statistical leadership for clinical studies
• Support DSMB and DMC statistical review
• Support regulatory submissions interactions
• Support statistical programming specifications

Perks/Benefits

• Career development
• Flexible work arrangements
• Fully remote
• Global collaboration
• Inclusive workplace culture
• Mentorship
• Training

Skills/Tech-stack

Analysis Plan | Analysis datasets | Biostatistics | Clinical Trial Design | Clinical trial | Clinical trials | Data Monitoring | Data Monitoring Committee | Data Safety | Data Safety Monitoring Board | Data safety monitoring | ICH Guidelines | Quality Control | R Programming | Randomization | Regulatory Submissions | Statistical Analysis | Statistical Analysis Plan | Statistical methodology | Statistical programming | Trial design