Remote Medical Writer for AI CSR & Trial Data (Contract)

mercor; United States; Remote; USD 124,000 - 207,000; Full time

Job summary

Mercor is seeking a Medical Writer for a remote contract role to generate and validate synthetic clinical trial data and to author CSR sections, prompts, and rubrics.

Requirements include a PhD or equivalent, 5+ years in pre-market (Phases 1–3) clinical trial data, long‑form authorship, and US or Canada residency, for about 20–25 hours/week.

Location is remote (US or Canada); compensation ranges from $90 to $150 per hour.

Qualifications

• 5+ years of experience in clinical trial data and CSR authorship.
• PhD or equivalent required.
• Comfortable with full-document, long-horizon authorship.

Responsibilities

• Generate and validate synthetic clinical trial data.
• Author CSR sections, prompts, golden outputs, and rubrics.
• Collaborate with AI research teams to improve data quality.

Skills

5+ years experience

Clinical trial data

Long-form authorship

Education

PhD or equivalent

Job description

Mercor is seeking a Medical Writer for a remote contract role to generate and validate synthetic clinical trial data and to author CSR sections, prompts, and rubrics.

Requirements include a PhD or equivalent, 5+ years in pre-market (Phases 1–3) clinical trial data, long‑form authorship, and US or Canada residency, for about 20–25 hours/week.

Location is remote (US or Canada); compensation ranges from $90 to $150 per hour.