Clinical Trial Writer - PhD

About the role

Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey.

This is a contract, remote position requiring 20–25 hours per week.

Responsibilities

• Generate and validate high-quality, synthetic clinical trial data.
• Author full Clinical Study Report (CSR) sections and design prompts, golden outputs, and rubrics.
• Quantify the ability of an AI agent in CSR task authorship.
• Work independently and asynchronously to meet deadlines.
• Collaborate with AI research teams to improve training data quality.

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.
• Must be located in the US or Canada.

Preferred Qualifications

• 10–25 years of experience.
• 30+ hours/week availability.

Pay

$90–$150/hour