Sr Principal Statistician
US - Home-Based, United States
R
USD 156K-234K Senior-level Full Time
Tasks
- Attend meetings with regulatory agencies
- Create statistical strategy for clinical trials
- Design clinical studies phase I to IV
- Develop and write statistical analysis plans
- Develop statistical programming for simulations and analysis
- Lead statistical aspects of study design
- Oversee analysis interpretation
- Perform and validate data analysis
- Prepare regulatory statistical documentation
- Produce clinical reports and integrated summaries
- Respond to statistical questions from regulators
- Review and input to data capture systems
- Validate CRO statistical deliverables
- Verify data accuracy and validity
Perks/Benefits
- 401k retirement savings plan
- Dental insurance
- Flexible Paid Vacation
- Medical insurance
- Vision insurance
Skills/Tech-stack
Adaptive Design | Analysis Plan | Bayesian statistics | CDISC | CDISC standards | Clinical Trial Design | Clinical trial | Data Analysis | Data Validation | Hypothesis Testing | ICH Guidelines | Nonparametric Models | Parametric Models | R | R Programming | SAS | SAS programming | Sample Size | Sample Size Calculation | Statistical Analysis | Statistical Analysis Plan | Statistical inference | Trial design
Education
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