Medical Writer, Clinical Trial Data and CSR
$90 - $150 per hourSaidGig
Role Overview
Contribute to clinical data and reporting workflows by generating and validating high-quality synthetic clinical trial data and authoring clinical study report content.
Key Responsibilities
- Generate and validate high-quality synthetic clinical trial data.
- Author complete sections of clinical study reports.
- Design prompts, reference outputs, and scoring rubrics to assess an AI agent''s ability to author CSR content.
Qualifications
- PhD or equivalent education.
- At least 5 years of relevant experience, with 10 to 25 years preferred.
- Experience with pre-market Phase 1, 2, and 3 clinical trial data and clinical study report authorship.
- Ability to manage full-document, long-horizon authorship.
Work Terms
- Remote, hourly engagement.
- 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.
Eligibility
Applicants must be located in the United States, Canada, or France.
Vacancy posted 6 hours ago
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