Reviews and refines AI-generated clinical study reports, regulatory dossier modules and medical affairs decks. Suits clinical research professionals with pharma, biotech or CRO experience who can work flexible remote hours.
About the role
About This Opportunity
We're working with a leading foundational AI lab to find experienced clinical research officers who can help train their latest language model on professional document, spreadsheet, and slide deck tasks.
We're looking for clinical research officers 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)
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
Official source: agent.askethos.com. Details can change; the platform's page is the final word. Something wrong with this listing? Tell us.
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