Sr/Principal Statistician
Tasks
- Conduct quality control and verification of study outputs
- Contribute to protocol design and randomization
- Coordinate study timelines and manage multiple studies
- Create mock tables listings figures
- Develop statistical analysis plans
- Lead statistical activities across clinical study lifecycle
- Mentor and coach biostatistics staff
- Provide statistical input for clinical trial documentation
- Review statistical programming outputs
- Serve as biostatistics representative on study teams
- Support regulatory interactions and integrated analyses
Perks/Benefits
- Career development opportunities
- Flexible working arrangements
- Mentoring opportunities
- Remote options
Skills/Tech-stack
Analysis Plan | Biostatistics | Clinical Practice | Clinical data | Clinical data management | Clinical study | Clinical study report | Clinical trial | Clinical trial protocol | Data Management | Data Quality | Data quality control | Good Clinical Practice | ICH Guidelines | Integrated Analysis | Quality Assurance | Quality Control | Randomization | SAS | Statistical Analysis | Statistical Analysis Plan | Statistical methodology | Statistical programming
Education
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