Associate Director Biostatistician Consultant (24 months contract)
Tasks
- Contribute to protocol design
- Contribute to study deliverable scheduling
- Design and prepare integrated safety and efficacy summaries
- Develop statistical analysis plans
- Draft protocols and amendments
- Lead study deliverables coordination
- Perform statistical analyses for final reports
- Perform statistical analyses for interim reports
- Represent biostatistics function for complex studies
- Support regulatory submission activities
Perks/Benefits
- N/A
Skills/Tech-stack
Analysis Plan | Clinical trial | Clinical trial analysis | Final Analysis | Integrated Summary | Integrated summary reporting | Interim analysis | Protocol Design | R | SAS | Statistical Analysis | Statistical Analysis Plan | Trial Analysis
Education
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