Medical Affairs Director – AI Training Consultant

About the role

Ethos is seeking an experienced Medical Affairs Director to support a leading AI lab in training its language model on professional medical documentation. The consultant will work remotely, creating and reviewing AI‑generated clinical study reports, protocol synopses, investigator brochures, regulatory dossier modules, and medical affairs slide decks.

Key responsibilities

• Author and review AI‑generated clinical study reports, protocol synopses, and regulatory dossier modules.
• Validate the scientific rigor of investigator brochures and medical affairs materials.
• Provide feedback to improve AI performance on document, spreadsheet, and slide‑deck tasks.
• Ensure compliance with ICH‑GCP standards and FDA/EMA regulatory expectations.
• Collaborate with the AI development team to refine training data and workflows.

Required profile

• 5+ years of experience in clinical research, biomedical science, or pharmaceutical/regulatory affairs.
• Direct 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 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 at $100 per hour.
• Flexible commitment of 5–20 hours per week (or more).
• Fully remote work schedule.
• Opportunity to shape cutting‑edge AI tools for the medical sector.