Disease-Area Clinician — Trial Endpoints & Prescribing
$150 - $230 / hour
Verified Mercor opportunity
As a medical writer on this project, you would own a part in multiple workflows: — 1. Clinical Data Generation — we need to generate and validate high-quality, synthetic clinical trial data. 2. CSR task authorship — you must be capable of authoring full CSR sections, and designing prompts, golden outputs, and rubrics to quantify the ability of an AI agent attempting to do the same thing. — To be qualified for this role, you must fit the following requirements: • Location: US, Canada, or France. • YOE: 5+ required. 10-25 preferred. • Education: PhD, or equivalent. • Hourly availability: 20-25 hours/week, minimum. 30+ preferred. • Experience: MUST have experience working with pre-market (Phases 1-3) clinical trial data and report authorship. Comfortable with full-document, long-horizon authorship.
This opportunity may suit professionals with relevant experience in AI evaluation, Clinical reasoning. Review the official description and requirements before applying.
The listing states $90 - $150 / hour. Confirm the final rate, workload, and payment terms during the official application process.
Before you apply
The listing states $90 - $150 / hour. Confirm the final rate, workload, and payment terms during the official application process.
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