Mercor
Mercor
Medical Writer
Medical Writer
US / CA / FR
Contract-based
Date Posted
Offered salary
$90 – $150 per hour
$90 – $150 per hour
Closing date
Closing soon
Closing soon
Qualification
PhD or equivalent
PhD or equivalent
Hiring location
US / CA / FR
US / CA / FR
Experience
5+ Years
5+ Years
Responsibilities
• Generate and validate high-quality synthetic clinical trial data
• Author full CSR sections and design prompts, golden outputs, and rubrics for AI evaluation
• Create evaluation tasks that measure AI ability to produce clinical trial reports
Requirements
• PhD or equivalent
• 5+ years of experience (10–25 years preferred) working with pre-market (Phases 1–3) clinical trial data and report authorship
• Comfortable with full-document, long-horizon authorship
• Based in the US, Canada, or France
• Available for 20–25 hours/week minimum (30+ preferred)
How to Apply
Click "Apply" to be taken to the Mercor website. Complete your profile by uploading your resume and confirming your work location. Once verified, you will be matched to opportunities as they arise. Please note that this role cannot support H1B or STEM OPT candidates. Applying through our link supports WFH Bulletin as a referral partner, but you are welcome to apply directly if you prefer.
Responsibilities
• Generate and validate high-quality synthetic clinical trial data
• Author full CSR sections and design prompts, golden outputs, and rubrics for AI evaluation
• Create evaluation tasks that measure AI ability to produce clinical trial reports
Requirements
• PhD or equivalent
• 5+ years of experience (10–25 years preferred) working with pre-market (Phases 1–3) clinical trial data and report authorship
• Comfortable with full-document, long-horizon authorship
• Based in the US, Canada, or France
• Available for 20–25 hours/week minimum (30+ preferred)
How to Apply
Click "Apply" to be taken to the Mercor website. Complete your profile by uploading your resume and confirming your work location. Once verified, you will be matched to opportunities as they arise. Please note that this role cannot support H1B or STEM OPT candidates. Applying through our link supports WFH Bulletin as a referral partner, but you are welcome to apply directly if you prefer.
Responsibilities
• Generate and validate high-quality synthetic clinical trial data
• Author full CSR sections and design prompts, golden outputs, and rubrics for AI evaluation
• Create evaluation tasks that measure AI ability to produce clinical trial reports
Requirements
• PhD or equivalent
• 5+ years of experience (10–25 years preferred) working with pre-market (Phases 1–3) clinical trial data and report authorship
• Comfortable with full-document, long-horizon authorship
• Based in the US, Canada, or France
• Available for 20–25 hours/week minimum (30+ preferred)
How to Apply
Click "Apply" to be taken to the Mercor website. Complete your profile by uploading your resume and confirming your work location. Once verified, you will be matched to opportunities as they arise. Please note that this role cannot support H1B or STEM OPT candidates. Applying through our link supports WFH Bulletin as a referral partner, but you are welcome to apply directly if you prefer.
Mercor
Medical Writer
Medical Writer
Overview
Overview
Mercor is recruiting Medical Writers to support AI training on clinical trial documentation. You will generate and validate synthetic clinical trial data, author full CSR sections, design prompts, create golden outputs, and build rubrics to evaluate AI performance. This is a remote contractor role requiring 20–25 hours/week (30+ preferred).
Mercor is recruiting Medical Writers to support AI training on clinical trial documentation. You will generate and validate synthetic clinical trial data, author full CSR sections, design prompts, create golden outputs, and build rubrics to evaluate AI performance. This is a remote contractor role requiring 20–25 hours/week (30+ preferred).
Mercor is recruiting Medical Writers to support AI training on clinical trial documentation. You will generate and validate synthetic clinical trial data, author full CSR sections, design prompts, create golden outputs, and build rubrics to evaluate AI performance. This is a remote contractor role requiring 20–25 hours/week (30+ preferred).
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Explore carefully reviewed remote job opportunities from trusted companies worldwide. Discover roles that match your skills, experience and work preferences all in one place.
Newsletter
Get Started
Find Verified Remote Jobs That Fit Your Career Goals
Explore carefully reviewed remote job opportunities from trusted companies worldwide. Discover roles that match your skills, experience and work preferences all in one place.
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© 2026 WFH Bulletin. All rights reserved.