Senior Medical Writer for AI-Driven Docs (Remote)

Ethos; United States; Remote; CAD 157,000 - 224,000; Full time

Job summary

Ethos is seeking senior medical writers with 5+ years in clinical research to help train an AI language model on professional documents, spreadsheets, and slide decks.

This fully remote role offers 5-20 hours per week with flexible start date ASAP, focusing on study reports, protocol synopses, investigator brochures, and regulatory materials.

Candidates must have direct experience authoring or reviewing such materials and strong regulatory knowledge.

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

Responsibilities

• Create, evaluate, and refine AI-generated documents, spreadsheets, and slide decks across core workflows: clinical study reports, protocol synopses, investigator brochures, and regulatory dossier modules
• Ensure accuracy, clarity, and regulatory alignment of medical writing outputs for AI model training

Skills

Clinical study reports

Protocol synopses

Regulatory dossiers

Job description

Ethos is seeking senior medical writers with 5+ years in clinical research to help train an AI language model on professional documents, spreadsheets, and slide decks.

This fully remote role offers 5-20 hours per week with flexible start date ASAP, focusing on study reports, protocol synopses, investigator brochures, and regulatory materials.

Candidates must have direct experience authoring or reviewing such materials and strong regulatory knowledge.