Requirements
Requires 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 scientific rigor in investigator brochures and medical affairs materials is essential. Expert-level document, spreadsheet, and slide craftsmanship with excellent written communication and attention to detail is also required.
Description
About This OpportunityWe'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/hourCommitment: Flexible, 5-20 hours per week (or more if desired)Location: Fully remote, work on your own scheduleStart date: ASAPQualifications 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 detailAbout EthosEthos 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 RequirementsDirect experience authoring or reviewing clinical study reports, protocol synopses, or regulatory dossier modules for a pharmaceutical, biotech, or CRO organizationDeep familiarity with ICH-GCP standards, FDA/EMA regulatory expectations, and the scientific rigor required in investigator brochures and medical affairs materialsExpert-level document, spreadsheet, and slide craftsmanship, with excellent written communication and attention to detail