Principal Statistician
Kent-R&D, United Kingdom
GBP 70K-80K (estimate) Senior-level Full Time
Tasks
- Apply advanced modeling techniques
- Conduct meta-analyses
- Contribute to publications and publication strategy
- Design clinical studies
- Develop statistical strategy
- Ensure compliance with ICH and GCP
- Ensure regulatory quality of statistical deliverables
- Lead blind data reviews
- Lead integrated analyses
- Oversee outsourced studies
- Perform data exploration
- Provide statistical input to study protocols
- Represent company in statistical regulatory discussions
- Respond to health authority queries
- Review statistical analysis plans
- Share best practices and knowledge
Perks/Benefits
Skills/Tech-stack
Adaptive Design | Analysis Plan | Biostatistics | CDISC | CRO oversight | Clinical Trial Methodology | Clinical data | Clinical data standards | Clinical trial | Data Standards | Experimental Design | GCP | Health Authority Communications | ICH Guidelines | Integrated Analysis | Meta-Analysis | Modeling | R | Regulatory Submissions | SAS | Statistical Analysis | Statistical Analysis Plan | Statistical inference | Statistics | Trial methodology
Education
Roles
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