Sr. Principal Biostatistician
Tasks
- Address statistical issues in regulatory settings
- Collaborate with medical writers on study reports
- Collaborate with statistical programmers and data management
- Conduct modeling and simulations
- Define statistical methodologies
- Develop analysis plans and report specifications
- Ensure integrity of randomization and CRFs
- Lead biostatistics representation on study teams
- Mentor biostatisticians
- Oversee study data analysis
- Participate in protocol development
- Perform statistical analysis for clinical development
- Prepare clinical study reports
- Provide statistical input to scientific discussions
- Review study setup activities
- Serve as peer reviewer and internal consultant
- Train and supervise contract statisticians
Perks/Benefits
Skills/Tech-stack
Biostatistics | Case Report Forms | Clinical Trial Methodology | Clinical trial | Data Analysis | R | Randomization | Regulatory Compliance | SAS | Simulation | Statistical Analysis | Statistical modeling | Statistical programming | Trial methodology
Education
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