Associate Director Biostatistician Consultant - Remote (24 months contract)
United States
R
USD 170K-218K (estimate) Mid-level Contract
Tasks
- Coordinate study deliverables
- Design clinical trial protocols
- Design integrated safety and efficacy summaries
- Develop statistical analysis plans
- Draft protocol amendments
- Generate final reports
- Generate interim reports
- Perform statistical analyses
- Present at study team meetings
- Support regulatory submission activities
Perks/Benefits
Skills/Tech-stack
Analysis Plans | Biostatistics | Clinical Trial Design | Clinical trial | Protocol development | R | Regulatory Submissions | SAS | Statistical Analysis | Statistical analysis plans | Trial design
Education
Language: en
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