Associate Director Biostatistics

Tasks

• Author and review statistical sections of regulatory documents
• Conduct simulation based analysis
• Contribute to statistical quality systems and data documentation
• Define estimands
• Design protocols and endpoints
• Determine sample size
• Develop SAP and TLF
• Ensure reproducibility and traceability
• Identify statistical and operational risks and propose mitigation
• Lead biostatistics for clinical and translational projects
• Mentor colleagues and support matrix leadership
• Oversee CROs and analytical vendors
• Oversee computational work and documentation
• Plan interim and adaptive decisions
• Translate clinical biological and regulatory questions into statistical plans

Perks/Benefits

• Annual bonus
• Commuting allowance
• Employee events
• Holiday allowance
• Pension plan
• Snacks and drinks
• Stock options
• Subsidized meals
• Vacation days

Skills/Tech-stack

Adaptive Design | Analysis Plan | Bayesian Methods | Clinical trials | Cloud Computing | Frequentist Methods | GCP | Precision Medicine | Python | R | Rare Disease Studies | Rare disease | Reproducible Research | Risk Management | SAS | Simulation | Statistical Analysis | Statistical Analysis Plan | Version control