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.
Medical Writer in Albertson at Unknown Company
This position is listed as full time and able to be worked remotely.