Senior Medical Writer: Clinical Trial CSR & Data Author

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.

We invite applications for the Senior Medical Writer:
Clinical Trial CSR & Data Author position located in San Francisco, CA, United States.

This opportunity is for the Senior Medical Writer:
Clinical Trial CSR & Data Author role at Mercor.

We are seeking a motivated Senior Medical Writer:
Clinical Trial CSR & Data Author to join Mercor in San Francisco, CA, United States.