Medical Writer

Role Overview

Contribute to clinical data generation and clinical study report development by producing high-quality synthetic clinical trial data and authoring substantive CSR content. This role also helps evaluate AI-generated CSR work through carefully designed prompts, reference outputs, and scoring rubrics.

Key Responsibilities

• Generate and validate high-quality synthetic clinical trial data.
• Author complete CSR sections.
• Create prompts, golden outputs, and rubrics to assess an AI agent''s ability to produce CSR content.

Qualifications

• PhD or equivalent education.
• At least 5 years of relevant experience, with 10 to 25 years preferred.
• Required experience with pre-market Phase 1, Phase 2, and Phase 3 clinical trial data and report authorship.
• Comfort with full-document, long-horizon authorship.

Work Terms

• Remote, hourly engagement.
• Must be located in the United States, Canada, or France.
• Availability of at least 20 to 25 hours per week is required; 30 or more hours per week is preferred.

Compensation

$90 to $150 per hour.