Senior Manager Biostatistician Consultant Remote in Canada - 24 months contract
Tasks
- Contribute to integrated summaries for safety and efficacy
- Coordinate study deliverables with statistical programmers and data managers
- Design early stage and late stage protocols
- Develop and write statistical analysis plans
- Draft protocols and protocol amendments
- Perform statistical analyses for interim and final reports
- Present and contribute statistics at study team meetings
- Provide department leadership and scheduling support
- Support regulatory submission activities
Perks/Benefits
Skills/Tech-stack
Analysis Plan | Biostatistics | Clinical trial | Clinical trial protocol | Integrated Summary | Interim analysis | R | Regulatory Submission | SAS | Statistical Analysis | Statistical Analysis Plan | Statistical programming
Education
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