Associate Director, Biostatistics
Princeton Pike - NJ, United States
R
USD 181K-220K (estimate) Mid-level Full Time
Tasks
- Coach and mentor team members
- Communicate data and quality mission and vision
- Conduct statistical analysis
- Create statistical analysis plans
- Design clinical trials
- Develop and advise team members
- Develop protocols
- Draft regulatory submissions
- Ensure adherence to standards
- Interpret clinical trial results
- Lead statistical community of practice
- Manage employee performance
- Manage multiple studies
- Prepare clinical study reports
- Present analysis results
- Review protocols and analysis plans
- Support publications and presentations
- Support regulatory requests
Perks/Benefits
- 401k plan
- Employee assistance program
- Flexible time off
- Global shutdown
- Identity Theft Benefit
- Legal support
- Life insurance
- Long-term disability
- Paid sick time
- Paid time off
- Paid volunteer days
- Short-term disability
- Summer Hours Flexibility
Skills/Tech-stack
Analysis planning | Clinical Study Reporting | Clinical study | Clinical trials | Clinical trials methodology | Data Manipulation | Graphing | Matrix Collaboration | Project Management | Protocol development | Python | R | Regulatory Interactions | Regulatory Submissions | SAS | Scientific Communication | Simulation | Statistical Analysis | Statistical Analysis Planning | Statistical Governance | Study reporting
Education
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