Expert Opportunity - Regulatory Affairs Specialist

About This Opportunity

Were working with a leading foundational AI lab to find experienced regulatory affairs specialists who can help train their latest language model on professional document, spreadsheet, and slide deck tasks.

Were looking for regulatory affairs specialists 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

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