Associate Director Biostatistician Consultant - Remote in Western EU(24 months contract)
Tasks
- Collaborate on study deliverable scheduling
- Contribute to protocol design
- Develop integrated safety and efficacy summaries
- Develop statistical analysis plans
- Draft protocols and amendments
- Perform interim and final statistical analyses
- Present statistical contributions at study meetings
- Represent biostatistics for complex studies
- Support regulatory submission activities
Perks/Benefits
Skills/Tech-stack
Analysis Plans | Biostatistics | Clinical trials | Final Analysis | Interim analysis | R | Regulatory Submissions | SAS | Statistical Analysis | Statistical analysis plans
Education
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