Director, Biostatistics
Cambridge, MA, United States
R
USD 206K-257K Executive-level Full Time
Tasks
- Author clinical study reports statistical methods
- Author statistics sections of clinical protocols
- Conduct statistical modeling
- Design randomization schedules
- Develop statistical analysis plans
- Lead statistical deliverables
- Mentor junior biostatisticians
- Perform QC and QA of statistical deliverables
- Perform exploratory statistical analyses
- Provide statistical input to data monitoring committee charters
- Represent company on statistical issues
- Respond to FDA and regulatory agency statistical comments
- Review analysis dataset specifications
- Review analysis plans and integrated summaries
- Review case report form designs
- Standardize biostatistics processes and improve workflows
- Support regulatory submission statistical activities
Perks/Benefits
Skills/Tech-stack
ADaM | Analysis Plans | Bayesian statistics | Biostatistics | CRO oversight | Clinical Trial Design | Clinical trial | Clinical trial analysis | Data Monitoring | Data Monitoring Committee | Data Validation | EAST | EMA regulations | EudraVigilance | FDA Regulations | Frequentist Statistics | ICH Guidelines | Interactive visualization | Python | QC QA | R | Randomization | SAS | SDTM | Statistical Analysis | Statistical analysis plans | Statistical modeling | Trial Analysis | Trial design
Education
Regions
Countries
States
Cities
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