Remote Clinical & Biomedical AI Training Specialist

Ethos; Dubai; Sur place; AED 430 000 - 582 000; Temps partiel

Résumé du poste

Ethos is seeking experienced clinical and biomedical specialists to train AI models on professional documents, spreadsheets, and slide decks. You will create, evaluate, and refine AI-generated materials across CSR, protocols, investigator brochures, and regulatory modules.

Ideal candidates have 5+ years in clinical research, biomedical science, or regulatory affairs with strong written communication and attention to detail. This is a flexible, remote role with 5-20 hours per week and ASAP start.

Qualifications

• Direct experience authoring or reviewing clinical study reports, protocol synopses, or regulatory dossier modules for pharma/biotech/CRO.
• Deep familiarity with ICH-GCP standards, FDA/EMA regulatory expectations, and scientific rigor 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 clinical and biomedical documents across core workflows (CSR, protocols, regulatory dossiers).
• Work with pharma/biotech/regulatory teams to ensure accuracy, compliance, and clarity of materials.
• Assess and improve document quality, consistency, and scientific rigor for publication plans and medical affairs decks.
• Collaborate with AI researchers to align outputs with regulatory expectations and industry standards.

Connaissances

Clinical study reports

Protocol synopses

Regulatory dossiers

ICH-GCP knowledge

Regulatory knowledge

Description du poste

Ethos is seeking experienced clinical and biomedical specialists to train AI models on professional documents, spreadsheets, and slide decks. You will create, evaluate, and refine AI-generated materials across CSR, protocols, investigator brochures, and regulatory modules.

Ideal candidates have 5+ years in clinical research, biomedical science, or regulatory affairs with strong written communication and attention to detail. This is a flexible, remote role with 5-20 hours per week and ASAP start.