Sr/Principal Statistician
Tasks
- Conduct quality control and verification
- Coordinate cross functional study teams
- Develop statistical analysis plans
- Lead statistical activities across clinical study lifecycle
- Mentor junior biostatistics staff
- Monitor project timelines and escalate risks
- Oversee statistical programming outputs
- Represent biostatistics on study teams
- Support protocol design and randomization
- Support regulatory interactions and integrated analyses
Perks/Benefits
- Career development opportunities
- Collaborative work culture
- Flexible working arrangements
- Mentorship opportunities
- Remote options
Skills/Tech-stack
Analysis Plans | Analysis planning | Biostatistics | Clinical Practice | Clinical Study Reporting | Clinical Trial Design | Clinical study | Clinical trial | Data Management | Good Clinical Practice | ICH Guidelines | Integrated Analysis | Quality Control | Randomization | Randomization Strategy | Regulatory Submissions | SAS | Statistical Analysis | Statistical Analysis Planning | Statistical analysis plans | Statistical methodology | Statistical programming | Study reporting | Trial design
Education
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