Sr/Principal Statistician (Sponsor-dedicated)

Tasks

• Contribute to quality control processes
• Develop randomization schedules
• Develop statistical analysis plans
• Lead statistical activities across clinical trial lifecycle
• Mentor junior statisticians
• Monitor project timelines and deliver statistical outputs
• Prepare mock tables listings and figures
• Provide statistical input into study design
• Review programming specifications datasets and outputs
• Serve as statistical representative on study teams
• Support case report form development
• Support regulatory submissions and inspection readiness
• Validate data outputs against SAPs

Perks/Benefits

• Family-friendly benefits
• Fully remote
• International collaboration
• Learning and development budget
• Paid leave
• Travel opportunities

Skills/Tech-stack

Analysis Plan | Biostatistics | Clinical Data Analysis | Clinical data | Clinical trials | Data Analysis | Data Validation | ICH Guidelines | Randomization | SAS | Statistical Analysis | Statistical Analysis Plan | Statistical programming