Senior Manager Biostatistician Consultant (remote in UK- Outside IR35) 24 months contract
Tasks
- Contribute to protocol design
- Coordinate study deliverables scheduling
- Develop integrated summaries for safety and efficacy
- Develop statistical analysis plans
- Draft protocols and amendments
- Perform statistical analyses for final reports
- Perform statistical analyses for interim reports
- Provide statistical contributions at study team meetings
- Support regulatory submission activities
Perks/Benefits
Skills/Tech-stack
Analysis Plan | Clinical trial | Integrated Summary | Interim analysis | Protocol | R | Regulatory Submissions | SAS | Statistical Analysis | Statistical Analysis Plan
Education
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