Principal Statistician - Early Phase

Tasks

• Build analysis datasets specifications
• Collaborate cross functional clinical data management programming regulatory teams
• Conduct quality control statistical deliverables
• Create statistical analysis plans SAPs
• Design randomization approaches
• Develop analysis strategies
• Lead clinical study statistical design
• Mentor biostatistics colleagues
• Perform statistical programming specifications review
• Prepare clinical study reports CSR
• Support DMC statistical input
• Support DSMB statistical input
• Support regulatory statistical activities

Perks/Benefits

• Career development
• Flexible work arrangements
• Fully remote
• International collaboration
• Mentorship
• Training opportunities

Skills/Tech-stack

Analysis Plan | Analysis dataset | Biostatistics | Clinical Trial Design | Clinical trial | DMC | DSMBB | Data Quality | ICH Guidelines | R Programming | Randomization | Regulatory Submissions | Statistical Analysis | Statistical Analysis Plan | Statistical methodology | Statistical programming | Trial design