Expert Opportunity - Senior Medical Writer ($100/hr, up to $2,000/week)

About This Opportunity We're working with a leading foundational AI lab to find experienced senior medical writers who can help train their latest language model on professional document, spreadsheet, and slide deck tasks. We're looking for senior medical writers with 5+ years in clinical research, biomedical science, or pharmaceutical/regulatory affairs to 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. Compensation: $100/hour Commitment: Flexible, 5-20 hours per week (or more if desired) Location: Fully remote, work on your own schedule Start date: ASAP 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 About Ethos Ethos is a new expert network built by a McKinsey/SoftBank/DeepMind team and backed by world-leading investors like General Catalyst. We connect experts with investors and consultancies for paid expert calls, speaking engagements, and advisory opportunities. Key Requirements 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

Create, evaluate, and refine AI-generated professional documents, spreadsheets, and slide decks to train a foundational AI language model. Focus areas include clinical study reports, protocol synopses, and regulatory dossier modules.

Requires 5+ years of experience in clinical research or pharmaceutical affairs with direct experience authoring regulatory documents. Must have deep familiarity with ICH-GCP standards and FDA/EMA regulatory expectations.

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Medical Writing
• Clinical Research
• Biomedical Science
• Pharmaceutical Regulatory Affairs
• Clinical Study Reports
• Protocol Synopses
• Investigator Brochures
• Regulatory Dossier Modules
• Medical Affairs
• Publication Planning
• ICH-GCP Standards
• FDA Regulatory Expectations
• EMA Regulatory Expectations
• Document Craftsmanship
• Spreadsheet Proficiency
• Slide Deck Creation

• Healthcare
• Science & Research
• Technology
• Consulting

Expérience minimale

5+ ans

Langue de l’offre

anglais

Heures de travail

20 heures par semaine

Niveau d’expérience

Mid-Senior level