Expert Opportunity - VP of Clinical Operations ($100/hr, up to $2,000/week)

Job summary

Train a language model by creating, evaluating, and refining AI-generated professional documents, spreadsheets, and slide decks. Focus areas include clinical study reports, protocol synopses, and regulatory dossier modules.

Job details

About This Opportunity We're working with a leading foundational AI lab to find experienced VPs of clinical operations who can help train their latest language model on professional document, spreadsheet, and slide deck tasks. We're looking for VPs of clinical operations 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

What you’ll do

Train a language model by creating, evaluating, and refining AI-generated professional documents, spreadsheets, and slide decks. Focus areas include clinical study reports, protocol synopses, and regulatory dossier modules.

Requirements

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.

Listed skills

• written communication · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

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

Job areas

• Healthcare
• Science & Research
• Management & Leadership
• Technology
• Consulting