Sr/Principal Statistician (Sponsor-dedicated)

Tasks

• Contribute to CRFs and clinical documentation
• Create mock tables listings figures
• Develop statistical analysis plans SAPs
• Lead statistical activities across clinical trial lifecycle
• Mentor junior statisticians and improve processes
• Monitor project timelines deliver statistical outputs
• Provide statistical input for study design and randomization
• Represent statistics on study teams
• Review and validate programming specifications datasets outputs
• Support quality control and regulatory submissions

Perks/Benefits

• Annual learning and development budget
• Family-friendly benefits
• Fully remote work
• Paid leave
• Travel for team meetings and events

Skills/Tech-stack

Analysis Plan | Clinical Data Analysis | Clinical Trial Methodology | Clinical data | Clinical trial | Clinical trial statistics | Data Analysis | ICH Guidelines | Randomization | Regulatory Submissions | SAS | Statistical Analysis | Statistical Analysis Plan | Study design | Trial methodology