Senior Medical Writer for AI-Regulatory Docs (Remote)

Ethos

New York (NY)

On-site

USD 114,000 - 162,000

Part time

14 days+
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Job summary

Ethos is working with a leading foundational AI lab to find experienced senior medical writers who can help train their latest language model on professional documents, spreadsheets, and slide deck tasks.

We seek candidates with 5+ years in clinical research, biomedical science, or pharma/regulatory affairs to create, evaluate, and refine AI-generated materials across clinical study reports, protocols, investigator brochures, regulatory dossiers, medical affairs slides, and publication plans.

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, regulatory dossier modules, medical affairs slide decks, and publication plans
  • Support training of a language model by providing high-quality, medically accurate inputs and reviews
  • Ensure alignment with ICH-GCP standards and regulatory expectations throughout all materials

Job description

Ethos is working with a leading foundational AI lab to find experienced senior medical writers who can help train their latest language model on professional documents, spreadsheets, and slide deck tasks.

We seek candidates with 5+ years in clinical research, biomedical science, or pharma/regulatory affairs to create, evaluate, and refine AI-generated materials across clinical study reports, protocols, investigator brochures, regulatory dossiers, medical affairs slides, and publication plans.

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