Biostatistician, Regulatory Submissions - Boston (2026 Start Date)
Tasks
- Advise on clinical trial design and analysis strategy
- Apply biostatistical methods to clinical development
- Communicate findings to technical and non-technical audiences
- Contribute to publications and presentations
- Develop analysis tools and programming standards
- Ensure reproducible analytical outputs
- Interpret analysis results
- Lead data integration cleaning and transformation
- Manage and mentor analysts and associates
- Oversee statistical analysis plans
- Support client relationships and business development
- Support regulatory documentation
- Support regulatory submissions
Perks/Benefits
- N/A
Skills/Tech-stack
ADaM | Analysis Plans | Biostatistics | Clinical Trial Design | Clinical trial | Clinical trials | Data Management | Data Transformation | Data cleaning | Evidence generation | Real-World Evidence | Regulatory science | SDTM | Statistical Analysis | Statistical analysis plans | Statistical programming | TLF Development | Trial design
Education
Bachelor of Science | Master of Arts | Master of Science | PhD
Regions
Countries
States
Cities
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