Role OverviewGenerate and validate high-quality, synthetic clinical trial data. Author full CSR sections and design prompts, golden outputs, and rubrics. Quantify the ability of an AI agent in CSR task authorship. Collaborate with AI research teams to improve training data quality.
What You Will Do
Work independently and asynchronously to meet deadlines.
Why It Might Be a Fit
Must have 5+ years of experience, PhD or equivalent, experience with pre-market (Phases 1-3) clinical trial data and report authorship, and be comfortable with full-document, long-horizon authorship.
Requirements
- 5+ years of experience
- PhD or equivalent
- Experience with pre-market (Phases 1-3) clinical trial data and report authorship
- Comfortable with full-document, long-horizon authorship
Benefits
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