Clinical Research Officer – Remote AI Training Expert

About the role

We are partnering with a leading AI lab to train its newest language model on professional clinical research documentation. The role is fully remote, flexible, and focused on creating, evaluating, and refining AI‑generated documents, spreadsheets, and slide decks.

Key responsibilities

• Produce and review AI‑generated clinical study reports, protocol synopses, and investigator brochures.
• Develop regulatory dossier modules and medical affairs slide decks.
• Assist in creating publication plans and related documentation.
• Ensure all outputs meet ICH‑GCP, FDA, and EMA standards.

Required profile

• 5+ years experience authoring or reviewing clinical study reports, protocol synopses, or regulatory dossier modules for pharma, biotech, or CRO organizations.
• Deep familiarity with ICH‑GCP standards and FDA/EMA regulatory expectations.
• Expert‑level craftsmanship in documents, spreadsheets, and slide presentations.
• Excellent written communication and meticulous attention to detail.

Required skills

• Regulatory dossier modules
• Clinical Study Reports
• Medical affairs materials
• EMA regulatory expectations
• Investigator brochures
• Protocol synopses
• ICH‑GCP standards

What we offer

• Compensation: $100 per hour
• Flexible commitment: 5–20 hours per week (or more)
• Fully remote work on your own schedule
• Immediate start date