Lead Statistician Clinical Trials - CDI- M/F
France - Toulouse - Langlade
EUR 64K-80K (estimate) Senior-level Full Time
Tasks
- Communicate findings to clinical regulatory partners
- Coordinate statistical submissions
- Design clinical trial protocols
- Determine sample size
- Develop safety efficacy pooled analysis
- Develop statistical analysis plan
- Draft study documents
- Ensure statistical documentation in eTMF
- Interpret results with clinicians
- Oversee CRO statistical deliverables
- Perform statistical analysis
- Support regulatory responses
- Validate statistical documents
- Write statistical sections of protocol
Perks/Benefits
Skills/Tech-stack
Adaptive trial designs | Bayesian Methods | Biomarker Data | CDISC | CRO Management | Clinical Trial Design | Clinical trial | Clinical trials | EMA guidelines | ETMF | FDA Guidelines | ICH Guidelines | Machine Learning | Multiple Testing Adjustment | Multiple testing | Oncology clinical trials | R | Real-World Evidence | SAS | Statistical Analysis | Trial design
Education
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