Associate Director Biostatistician Consultant - Remote in UK (24 months contract)
Tasks
- Analyze integrated safety and efficacy summaries
- Contribute to protocol design
- Design integrated safety and efficacy summaries
- Develop statistical analysis plans
- Draft protocols and amendments
- Lead planning of study deliverables
- Perform statistical analyses for final reports
- Perform statistical analyses for interim reports
- Provide statistical input at project level meetings
- Provide statistical input at study team meetings
- Represent biostatistics function for complex studies
- Support regulatory submission activities
Perks/Benefits
- N/A
Skills/Tech-stack
Analysis Plan | Biostatistics | Clinical trial | Clinical trial protocol | Efficacy analysis | Final Analysis | Integrated Summaries | Interim analysis | R | Regulatory Submissions | SAS | Safety Analysis | Statistical Analysis | Statistical Analysis Plan
Education
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