Associate Director - Biostatistician in Statistical Methodology
UK - Cambridge, United Kingdom
GBP 38K-45K (estimate) Mid-level Full Time
Tasks
- Analyze complex genomic proteomic and imaging data
- Collaborate with scientists and regulators through publications and presentations
- Consult on statistical issues for cross functional teams
- Contribute to clinical study reports
- Create pragmatic solutions for clinical study design
- Design biomarker guided clinical trials
- Determine power and sample size for subgroups
- Develop and implement innovative statistical methods
- Develop statistical analysis plans
- Lead capability building for statistical methodology
- Perform statistical analysis and interpretation for clinical trials
- Provide statistical input for drug development
- Validate diagnostic assays
- Write regulatory reports for FDA and EMA
Perks/Benefits
- Flexible working schedule
- In person collaboration at least three days per week
- Reasonable accommodations for candidates
Skills/Tech-stack
Adaptive trial design | Analysis Plan | Bayesian Methods | Biomarker Discovery | Biomarker Validation | Biomarker guided trial design | Biostatistics | Clinical Trial Design | Clinical trial | Data Analysis | EMA | FDA | Genomic Data Analysis | Genomic data | Imaging Data Analysis | Imaging data | Power analysis | Proteomic data | Proteomic data analysis | R | Regression Analysis | Regulatory Reporting | SAS | Sample Size | Sample Size Determination | Simulation | Statistical Analysis | Statistical Analysis Plan | Statistical modeling | Trial design
Education
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