Mercor in Toronto, Canada is seeking a part time medical writer to shape synthetic clinical trial data and CSR sections across Phases 1–3. You will generate high-quality data, validate it, and design prompts, rubrics, and golden outputs to measure AI performance in CSR tasks.
The ideal candidate has a PhD, 5+ years of relevant experience, and is comfortable with long-form, full-document authorship on pre-market data. 20–25 hours per week are required, with 30+ preferred.
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📌 Senior Medical Writer – Ai Driven Csr & Trial Data New Brunswick (Canada)
🏢 Mercor
📍 Canada
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