Senior Medical Writer: Clinical Trial CSR & Data Author

Mercor; San Francisco (CA); Remote; USD 83,000 - 124,000; Full time

Job summary

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.

Qualifications

• 5+ years of experience in medical writing and data generation for clinical trials.
• Experience with pre-market (Phases 1-3) data and report authorship is mandatory.
• Location: US, Canada, or France; part-time availability 20–25 hrs/week, 30+ ideal.

Responsibilities

• Clinical Data Generation — generate and validate high-quality, synthetic clinical trial data.
• CSR task authorship — author CSR sections, design prompts, gold outputs, and rubrics to quantify AI agent performance.

Skills

Medical writing

CSR writing

Prompt design

Clinical data generation

Education

PhD or equivalent

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.