Biostatistician, Regulatory Submissions
Tasks
- Apply biostatistical methods to clinical development
- Communicate findings to technical and non-technical audiences
- Contribute to clinical trial design and analysis strategy
- Develop analysis tools and best practices
- Ensure reproducible analytical outputs
- Implement statistical programming standards
- Manage and mentor analysts
- Oversee statistical analysis plans
- Perform data integration cleaning and transformation
- Support business development and client relationships
- Support regulatory submissions
- Support research dissemination via publications presentations and regulatory documentation
Perks/Benefits
- N/A
Skills/Tech-stack
ADaM | Analysis Plan | Biostatistics | Clinical Trial Design | Clinical trial | Data Transformation | Data cleaning | Data integration | FDA | Real-World Evidence | Regulatory Submissions | SDTM | Statistical Analysis | Statistical Analysis Plan | Statistical programming | TLF Development | Trial design
Education
Regions
Countries
States
Cities
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