Biostatistician, Regulatory Submissions (2026 Start Date)
Boston, MA, United States
USD 210K-255K Mid-level Full Time
Tasks
- Apply biostatistical methods
- Communicate findings to technical and non-technical audiences
- Contribute to publications presentations and regulatory documentation
- Develop analysis strategy
- Develop programming standards and best practices
- Ensure reproducible analytical outputs
- Integrate clean transform clinical trial data
- Manage and mentor analyst teams
- Oversee statistical analysis plan implementation
- Support business development and client relationships
- Support regulatory submissions
Perks/Benefits
- N/A
Skills/Tech-stack
ADaM | Biostatistics | Clinical Trial Data | Clinical Trial Design | Clinical trial | Data Transformation | Data cleaning | EMA | Evidence generation | FDA | Post Marketing Evidence Generation | Programming Standards | Real-World Evidence | Regulatory Submissions | SDTM | Statistical Analysis | Statistical programming | TLF | Trial data | Trial design
Education
Roles
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Countries
States
Cities
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