Sr/Principal Statistician

Tasks

• Contribute to protocol design and randomization
• Coordinate study timelines and deliverables
• Create mock tables listings and figures
• Develop statistical analysis plans
• Ensure study output quality control and verification
• Lead statistical activities across clinical study lifecycle
• Mentor junior biostatistics staff
• Oversee and review statistical programming outputs
• Provide statistical input for clinical trial documentation
• Serve as biostatistics representative on study teams
• Support regulatory interactions and submissions

Perks/Benefits

• Career development opportunities
• Collaborative work culture
• Flexible working arrangements
• Mentoring opportunities
• Remote options

Skills/Tech-stack

Analysis planning | Clinical Practice | Clinical study | Clinical study report | Clinical trial | Clinical trial protocols | DMC | DSMB | Data Monitoring | Data Monitoring Committees | Good Clinical Practice | ICH | Integrated Analysis | Quality Control | Randomization | SAS | Statistical Analysis | Statistical Analysis Planning | Statistical methodology | Statistical quality | Statistical quality control