About this opportunity
Mercor lists this Senior Medical Writer: Clinical Trial CSR & Data Author opportunity in san francisco, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Mercor is seeking a part-time medical writer to own portions of clinical data generation and CSR task authorship. You will generate and validate synthetic trial data and design prompts, rubrics, and golden outputs to assess AI-driven CSR work.
The role requires 5+ years in medical writing with PhD or equivalent, and experience with pre-market trial data. Location options include US, Canada, or France, with 20–25 hours/week minimum and greater availability preferred.
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Worksite address
san francisco, CA, 94199, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.