Biostatisticien H/F

Tasks

• Analyze clinical studies
• Contribute to clinical and statistical protocol design
• Develop statistical analysis plan
• Develop statistical models
• Ensure technical compliance of infrastructure
• Interpret and communicate study results
• Maintain and develop business software tools
• Manage secure server environment and access
• Monitor ongoing clinical studies
• Provide IT interface for deployments maintenance and security
• Stay updated on methodological and scientific advances
• Support publications and posters
• Validate and evolve eCRF EDC and CTMS tools
• Write and validate statistical sections of clinical documents

Perks/Benefits

• N/A

Skills/Tech-stack

Analysis Plan | Biostatistics | CTMS | Clinical Trial Design | Clinical trial | ECRF | EDC | JavaScript | Prediction models | Python | R | S&OP | SAS | SQL | Sample Size | Sample Size Calculation | Statistical Analysis | Statistical Analysis Plan | Statistical modeling | Trial design