Biostatistician

• Design and author expert-level evaluation tasks simulating real-world biostatistics challenges, such as clinical trial analysis, regulatory submission reviews, and observational study assessments.
• Source, construct, and curate authentic datasets including trial data, patient records, and protocol documents for task use.
• Define correct methodological solutions and defensible clinical interpretations for each evaluation scenario.
• Develop comprehensive, 35+ item rubrics to evaluate AI agent performance with respect to methodological rigor and clinical reasoning.
• Ensure all tasks reflect the complexity and depth of real-world biostatistics practice, avoiding simplified or textbook-style examples.
• Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific standards.

• No prior experience in AI is required — your domain knowledge is what matters.
• Demonstrated command of clinical study design, regulatory documentation, and observational research methodologies.
• Strong attention to methodological detail, clinical interpretation, and regulatory sensitivity.
• Excellent written communication skills and ability to author detailed grading rubrics and technical documentation.

• Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a plus.

Project and contracting process: micro1. Applications continue on the provider's website.