About This Opportunity
We're working with a leading foundational AI lab to find experienced heads of regulatory affairs who can help train their latest language model on professional document, spreadsheet, and slide deck tasks.
We're looking for heads of regulatory affairs 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
Versátil, 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 det
📌 Expert Opportunity (España)
🏢 ETHOS
📍 España