Principal Statistician - Ophthalmology

Tasks

• Contribute to database design and analysis datasets specifications
• Create statistical deliverables including tables listings figures
• Develop review and oversee statistical analysis plans
• Lead statistical activities for clinical trials
• Mentor biostatistics professionals and lead training
• Participate in DSMB and DMC statistical oversight
• Perform statistical quality control and independent review
• Support R based statistical programming
• Support integrated analyses and regulatory submissions
• Support protocol randomization and clinical study report preparation

Perks/Benefits

• Career development
• Collaborative & Inclusive Culture
• Flexible work environment
• Fully remote Europe
• Mentoring and supportive line management
• Peer recognition
• Training access

Skills/Tech-stack

Analysis Plan | Clinical study | Clinical study report | Clinical trials | Data Monitoring | Data Monitoring Committee | Data Safety | Data Safety Monitoring Board | Data safety monitoring | ICH E9 | ICH Guidelines | Integrated Analysis | Quality Control | R | Randomization | Regulatory Submissions | SOPs | Statistical Analysis | Statistical Analysis Plan | Statistical Study Design | Statistical programming | Study design