Remote Clinical & Biomedical Specialist for AI Docs

Ethos; United States; À distance; USD 23 000 - 91 000; Temps partiel

Avantages offerts par ce poste

Health insurance

Résumé du poste

Ethos is seeking experienced clinical and biomedical specialists to help train an AI language model on professional documents, spreadsheets, and slide decks across core workflows.

This fully remote engagement offers flexible hours (5–20 per week) at $100/hour, with potential for more. Candidates should have 5+ years in clinical research, regulatory affairs, or biomedical science and strong document craftsmanship with attention to detail.

Qualifications

• Direct experience authoring or reviewing clinical study reports, protocol synopses, or regulatory dossier modules for a pharmaceutical, biotech, or CRO organization
• 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

Responsabilités

• Create, evaluate, and refine AI-generated documents, spreadsheets, and slide decks across core workflows: clinical study reports, protocol synopses, investigator brochures, regulatory dossier modules, medical affairs slide decks, and publication plans.
• Collaborate with subject-matter experts to ensure accuracy and regulatory compliance of produced materials
• Maintain high quality and consistency across all AI-assisted documents, spreadsheets, and decks

Connaissances

Written communication

Attention to detail

Regulatory affairs knowledge

ICH-GCP familiarity

Formation

5+ years in clinical research, biomedical science, or pharmaceutical/regulatory affairs

Description du poste

Ethos is seeking experienced clinical and biomedical specialists to help train an AI language model on professional documents, spreadsheets, and slide decks across core workflows.

This fully remote engagement offers flexible hours (5–20 per week) at $100/hour, with potential for more. Candidates should have 5+ years in clinical research, regulatory affairs, or biomedical science and strong document craftsmanship with attention to detail.