Senior Medical Writer for AI-Regulatory Docs (Remote)

Ethos

New York (NY)

Remote

USD 114,000 - 162,000

Part time

14 days+

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

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.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Senior Medical Writer for AI-Driven Docs (Remote)
Senior Medical Writer for AI-Driven Docs (Remote)

Ethos • United States

Remote
CAD 157,000 - 224,000
Remote Regulatory Affairs Specialist for AI Docs
Remote Regulatory Affairs Specialist for AI Docs

Ethos • United States

Remote
USD 138,000 - 165,000
Remote Clinical Research Scientist-AI Doc & Slide Training
Remote Clinical Research Scientist-AI Doc & Slide Training

Ethos • United States

Remote
USD 114,000 - 162,000
Remote Medical Affairs Director - AI-Driven Clinical Docs
Remote Medical Affairs Director - AI-Driven Clinical Docs

Ethos • United States

Remote
CAD 117,000 - 158,000
Senior Medical Writer: Regulatory AI Clinical Docs (Remote)
Senior Medical Writer: Regulatory AI Clinical Docs (Remote)

Executive Staff Recruiters / ESR Healthcare • New York (NY)

Remote
USD 90,000 - 135,000
Remote Clinical Research Associate for AI Document Training
Remote Clinical Research Associate for AI Document Training

Ethos • United States

Remote
AUD 165,000 - 223,000
Remote Medical Writer for AI-Driven Clinical Documents
Remote Medical Writer for AI-Driven Clinical Documents

Remotebridge • United States

Remote
USD 110,000 - 150,000
Clinical Research Scientist - AI Doc & Deck Training Remote
Clinical Research Scientist - AI Doc & Deck Training Remote

Ethos • New York (NY)

Remote
USD 114,000 - 162,000
Remote Pharma Medical Writer for AI-Regulatory Evaluation
Remote Pharma Medical Writer for AI-Regulatory Evaluation

Medcruit Limited • United States

Remote
USD 58,000 - 115,000
Remote work
Remote VP, AI-Powered Clinical Operations Leader
Remote VP, AI-Powered Clinical Operations Leader

Ethos • United States

Remote
USD 114,000 - 162,000