Remote Medical Writer for AI Trial Data (Part-Time)

mercor; San Francisco (CA); Hybrid; CAD 177.000 - 294.000; Vollzeit

Zusammenfassung

Mercor is seeking a Medical Writer to generate and validate synthetic clinical trial data, author CSR sections, and design prompts and rubrics. The role requires 5+ years of experience and a PhD or equivalent, with experience in pre-market trial data and long-form document authorship.

The position is remote, contract-based, and demands 20–25 hours per week, offering an opportunity to collaborate with AI research teams to improve data quality.

Qualifikationen

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

Aufgaben

• Generate and validate synthetic clinical trial data.
• Author CSR sections, design prompts, golden outputs, and rubrics.
• Quantify AI agent performance in CSR task authorship.
• Work independently and meet deadlines.
• Collaborate with AI research teams to improve training data quality.

Kenntnisse

Clinical data experience

CSR writing

AI data quality

Ausbildung

PhD or equivalent

Jobbeschreibung

Mercor is seeking a Medical Writer to generate and validate synthetic clinical trial data, author CSR sections, and design prompts and rubrics. The role requires 5+ years of experience and a PhD or equivalent, with experience in pre-market trial data and long-form document authorship.

The position is remote, contract-based, and demands 20–25 hours per week, offering an opportunity to collaborate with AI research teams to improve data quality.