Senior Manager Biostatistician Consultant Remote in US (24 months contract)
Tasks
- Collaborate with statistical programmers and data managers
- Contribute to protocol design
- Design integrated summaries for safety and efficacy
- Develop statistical analysis plans
- Draft protocols and amendments
- Lead study deliverable scheduling
- Perform statistical analyses for final reports
- Perform statistical analyses for interim reports
- Present statistical contributions at study team meetings
- Support regulatory submission activities
Perks/Benefits
Skills/Tech-stack
Analysis Plan | Clinical trial | Clinical trial protocols | Final Reporting | Integrated Summary | Interim Reporting | R | Regulatory Submissions | SAS | Statistical Analysis | Statistical Analysis Plan
Education
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