Director, Biostatistics
Cambridge, MA, United States
USD 206K-257K Executive-level Full Time
Tasks
- Author clinical study report statistics methods
- Author statistical analysis plans
- Collaborate with clinical medical regulatory teams
- Conduct exploratory statistical analyses
- Conduct statistical modeling
- Contribute to publications
- Design randomization schedules
- Lead process improvement for biostatistics
- Lead statistical deliverables coordination
- Mentor junior biostatisticians
- Oversee CRO statistical services
- Perform QC QA of statistical deliverables
- Provide statistical input for DMC charters
- Respond to FDA regulatory comments
- Review IRB EC comments
- Review analysis dataset specifications
- Review case report form designs
- Review clinical protocol statistics sections
- Review test randomization lists
- Support regulatory submission statistical activities
Perks/Benefits
Skills/Tech-stack
ADaM | Analysis Dataset Specification | Analysis Plan | Analysis dataset | Bayesian statistics | Biostatistics | Clinical trials | Data Visualization | Dataset specification | EAST | Frequentist Statistics | Python | QC QA | R | Randomization | SAS | SDTM | Statistical Analysis | Statistical Analysis Plan | Statistical modeling
Education
Roles
Biostatistician | Biostatistics | Director | Director, Biostatistics
Regions
Countries
States
Cities
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