Principal Biostatistician
United States-New Jersey-Remote, United States
R
USD 123K-198K (estimate) Senior-level Full Time
Tasks
- Attend and contribute to client meetings
- Contribute to Data Monitoring Committee activities
- Interact with clients and regulatory authorities
- Lead production and quality control of reports
- Perform sample-size calculations and develop analysis plans
- Provide statistical support for trial design and analysis
- Review clinical reports and publications
- Support business development and study design discussions
- Understand regulatory requirements and statistical methodologies
Perks/Benefits
Skills/Tech-stack
Communication | Data Monitoring | GCP | ICH Guidelines | Leadership | Project Management | Regulatory Compliance | SAS programming | Sample Size Calculation | Statistical Analysis | Trial design
Education
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