Clinical Research Scientist – AI Training

About the role

Ethos is partnering with a leading AI lab to train a new language model on professional clinical research documents, spreadsheets, and slide decks. The role involves creating, evaluating, and refining AI‑generated outputs for core workflows such as clinical study reports, protocol synopses, investigator brochures, regulatory dossier modules, and medical affairs materials.

Key responsibilities

• Author and review AI‑generated clinical study reports, protocol synopses, and regulatory dossier modules.
• Ensure documents meet ICH‑GCP standards and FDA/EMA regulatory expectations.
• Produce high‑quality medical affairs slide decks and publication plans.
• Collaborate remotely with the AI research team to improve model performance.

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 a pharma, biotech, or CRO organization.
• Deep familiarity with ICH‑GCP standards and FDA/EMA regulatory expectations.

Required skills

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