Sr/Principal Statistician (Sponsor-dedicated)

Tasks

• Contribute to quality control and regulatory submission readiness
• Create mock tables listings and figures
• Develop randomization schedules
• Develop statistical analysis plans
• Ensure compliance with statistical analysis plans
• Lead statistical activities across clinical trial lifecycle
• Manage project timelines delivery of statistical outputs
• Provide statistical input to study design
• Review validate programming specifications datasets and outputs
• Serve as statistical representative on study teams
• Support mentorship of junior statisticians

Perks/Benefits

• Family-friendly benefits
• Fully remote work
• Global clinical trials exposure
• International collaboration opportunities
• Learning and development budget
• Paid leave
• Travel for team meetings

Skills/Tech-stack

Analysis Plans | Biostatistics | Clinical Trial Methodology | Clinical data | Clinical trial | ICH Guidelines | Quality Control | Randomization | Regulatory Submissions | SAS | Statistical Analysis | Statistical analysis plans | Statistical programming | Study design | Trial methodology