Biostatistician, Regulatory Submissions (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 research dissemination through publications and presentations
- Develop tools programming standards and best practices
- Direct data integration cleaning and transformation
- Manage and mentor analysts and associates
- Oversee statistical analysis plans implementation
- Support business development and client relationships
- Support regulatory documentation
- Support regulatory submissions and evidence generation
Perks/Benefits
- N/A
Skills/Tech-stack
ADaM | Analysis Plan | Biostatistics | Clinical Trial Design | Clinical trial | EMA | FDA | PAES | PASS | Real-World Evidence | Regulatory Submissions | SDTM | Statistical Analysis | Statistical Analysis Plan | Statistical programming | TLF Development | Trial design
Education
Roles
Analyst | Biostatistician | Clinical Data Analyst | Data Analyst
Regions
Countries
States
Cities
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