Medical Writer - Fully Remote | Upto $150/hr

mercor; San Francisco (CA); Hybrid; CAD 177,000 - 294,000; Full time

Job summary

Mercor is seeking a Medical Writer to generate and validate synthetic clinical trial data, author CSR sections, and design prompts and rubrics. The role requires 5+ years of experience and a PhD or equivalent, with experience in pre-market trial data and long-form document authorship.

The position is remote, contract-based, and demands 20–25 hours per week, offering an opportunity to collaborate with AI research teams to improve data quality.

Qualifications

• 5+ years of experience in clinical data or CSR writing.
• PhD or equivalent required.
• Experience with pre-market clinical trial data and report authorship.
• Comfortable with full-document, long-horizon authorship.

Responsibilities

• Generate and validate synthetic clinical trial data.
• Author CSR sections, design prompts, golden outputs, and rubrics.
• Quantify AI agent performance in CSR task authorship.
• Work independently and meet deadlines.
• Collaborate with AI research teams to improve training data quality.

Skills

Clinical data experience

CSR writing

AI data quality

Education

PhD or equivalent

Job description

About the job

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 .

Position: Medical Writer
Type: Contract
Compensation: $90–$150/hour
Location: Remote
Commitment: 20–25 hours/week

Role Responsibilities

• 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.

Qualifications Preferred

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