Principal Statistician - PVH
Tasks
- Analyze and interpret clinical trial data
- Calculate sample size and power
- Contribute to regulatory submission sections
- Design clinical study biostatistics components
- Develop and validate analysis programs
- Lead statistical process improvements and standardization
- Respond to FDA and regulatory agency questions
- Review protocol and case report forms
- Summarize data in tables and figures
- Support regulatory review and approval
- Write results and methods sections of reports
- Write statistical analysis plan
- Write statistical portions of protocols
Perks/Benefits
Skills/Tech-stack
Adaptive trial design | Analysis Plan | Bayesian Methods | Biostatistics | Clinical Practice | Clinical Trial Design | Clinical trial | Data Analysis | Data Integrity | Data Validation | Good Clinical Practice | Group sequential methods | Interim analysis | Longitudinal analysis | Missing Data Analysis | Missing data | Mixed Models | Multiple testing | Power calculation | R | Regression Modeling | Regulatory Compliance | Regulatory Submissions | SAS | Sample Size | Sample Size Calculation | Statistical Analysis | Statistical Analysis Plan | Statistical inference | Statistical programming | Survival analysis | Trial design
Education
Bachelor of Science | Master of Science | Master of Science in Biostatistics | PhD | PhD in Statistics
Roles
Biostatistician | Principal | Principal Statistician | Statistician
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