Remote Clinical Research Associate for AI Document Training

Ethos; United States; Remote; AUD 165,000 - 223,000; Part time

Job summary

Ethos is seeking experienced clinical research associates to help train AI models on professional documents, spreadsheets, and slide decks. This fully remote role offers flexible 5–20 hours per week and a competitive hourly rate.

Ideal candidates have 5+ years in clinical research, biomedical science, or regulatory affairs and can produce high-quality, regulation-compliant materials across study reports, protocols, and regulatory dossiers.

Qualifications

• 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, FDA/EMA regulatory expectations, and the scientific rigor required in investigator brochures and medical affairs materials.
• Expert-level document, spreadsheet, and slide craftsmanship, with excellent written communication and attention to detail.

Responsibilities

• Create, evaluate, and refine AI-generated clinical research documents, spreadsheets, and slide decks.
• Develop materials across core workflows: clinical study reports, protocol synopses, investigator brochures, regulatory dossiers, and publication plans.
• Ensure quality, accuracy, and regulatory compliance while collaborating with cross-functional teams.

Skills

Clinical study reports

ICH-GCP/regulatory knowledge

Document/spreadsheet/slide craft

Job description

Ethos is seeking experienced clinical research associates to help train AI models on professional documents, spreadsheets, and slide decks. This fully remote role offers flexible 5–20 hours per week and a competitive hourly rate.

Ideal candidates have 5+ years in clinical research, biomedical science, or regulatory affairs and can produce high-quality, regulation-compliant materials across study reports, protocols, and regulatory dossiers.