Data annotation job
Medical Writer
Mercor · Posted 2 weeks ago
$90 to $150/hrRemote (multiple countries)Contract
- LLM training
- Healthcare
- STEM
About this role
As a medical writer on this project, you would own a part in multiple workflows:
- Clinical Data Generation, we need to generate and validate high-quality, synthetic clinical trial data.
- 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 listing is aggregated by DataAnnotationJobs.org. Applications are processed by Mercor, not by this site.
Mercor is an AI-native talent marketplace connecting vetted domain experts such as doctors, lawyers, and engineers directly with frontier AI labs for RLHF, evaluation, and specialized training data at massive scale. See all Mercor jobs.
Apply for this role
Your details first, then a short screening test. Both are read as part of your application and go to Mercor, and we will tell you when similar roles appear.