Sr/Principal Statistician
Tasks
- Conduct quality control of study outputs
- Contribute to protocol design and randomization
- Coordinate project timelines and manage multiple studies
- Develop statistical analysis plans
- Lead statistical activities across clinical study lifecycle
- Mentor and coach junior biostatistics staff
- Oversee statistical programming outputs
- Serve as biostatistics representative on study teams
- Support regulatory interactions and integrated analyses
Perks/Benefits
- Career development opportunities
- Collaborative work culture
- Flexible working arrangements
- Mentoring opportunities
- Remote options
Skills/Tech-stack
Analysis Plans | Analysis planning | Biostatistics | Clinical Practice | Clinical Trial Data | Clinical study | Clinical study report | Clinical trial | Clinical trial data management | Cross-Functional Collaboration | Cross-functional | DSMB | Data Management | Data Monitoring | Data Monitoring Committee | Functional collaboration | Good Clinical Practice | ICH Guidelines | Integrated Analysis | Protocol development | Quality Control | Randomization | SAS | Statistical Analysis | Statistical Analysis Planning | Statistical analysis plans | Statistical methodology | Statistical programming | Study design | Trial Data Management
Education
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