Sr/Principal Statistician (Sponsor-dedicated)

Tasks

• Create mock tables listings and figures
• Develop statistical analysis plans
• Lead statistical activities across clinical trial lifecycle
• Mentor junior biostatisticians and improve processes
• Monitor project timelines and deliver statistical outputs
• Provide statistical input to study design randomization schedules and CRFs
• Review validate programming specifications datasets and outputs
• Serve as statistical representative on study teams
• Support quality control and regulatory submissions

Perks/Benefits

• Exposure to global clinical trials
• Family-friendly benefits
• Fully remote
• International collaboration
• Learning and development budget
• Paid leave
• Travel opportunities

Skills/Tech-stack

Analysis Plan | Biostatistics | CRF | Clinical Trial Design | Clinical data | Clinical trial | Data Validation | ICH Guidelines | Quality Control | Randomization | SAS | Statistical Analysis | Statistical Analysis Plan | Trial design