[Hiring] Clinical Trial Writer @Mercor

Role Description

• Generate and validate high-quality, synthetic clinical trial data.
• Author full 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.

Qualifications

• Must-Have:
• 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.
• Location: US or Canada.
• Preferred:
• 10–25 years of experience.
• 30+ hours/week availability.

Company Description

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.