Sr/Principal Statistician
Tasks
- Conduct quality control and verification of statistical outputs
- Coordinate and review biostatistics and programming work
- Develop statistical analysis plans
- Lead statistical activities across clinical study lifecycle
- Mentor and coach biostatistics staff
- Monitor project timelines and escalate risks
- Oversee and review statistical programming outputs
- Prepare analysis planning deliverables
- Serve as biostatistics representative on study teams
- Support protocol design and randomization
- Support regulatory interactions and integrated analyses
Perks/Benefits
- Career development opportunities
- Flexible working arrangements
- Mentorship opportunities
- Remote work options
Skills/Tech-stack
Analysis Plans | Analysis planning | Clinical Practice | Clinical Trial Design | Clinical study | Clinical study report | Clinical trial | Data Quality | Data quality control | Good Clinical Practice | ICH Guidelines | Integrated Analysis | Quality Control | Randomization | SAS programming | Statistical Analysis | Statistical Analysis Planning | Statistical analysis plans | Statistical methodology | Trial design
Education
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