Associate Director of Biostatistics
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Job Summary
Collaborating with cross-functional development teams, the full-time Associate Director of Biostatistics will contribute to trial design, protocol development, and regulatory submissions while managing multiple studies to ensure adherence to standards.
Key responsibilities
- Collaborates in the design of innovative clinical trials and contributes to project development strategy
- Independently authors and reviews protocols, statistical analysis plans, and clinical study reports
- Provides statistical support and leadership for health authority requests and public releases of information
Required qualifications
- PhD (6+ years) or MS (8+ years) in statistics, biostatistics, or a related field with experience in clinical trials
- Proficiency in scientific computing/programming (SAS, R, or Python) for advanced statistical analysis
- Expertise in statistical/clinical trials methodology relevant to clinical development
- Good understanding of the regulatory landscape and experience in regulatory interactions
- Demonstrated leadership abilities and project management skills
Complete Job Description
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