Expert Opportunity - Clinical Research Scientist ($100/hr, up to $2,000/week)
Create, evaluate, and refine AI-generated professional documents, spreadsheets, and slide decks for a foundational AI lab. Focus areas include clinical study reports, protocol synopses, and regulatory dossier modules.
- Remote
- Canada
- Posted Sep 6, 2026
- 1 position
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Job summary
About This Opportunity We're working with a leading foundational AI lab to find experienced clinical research scientists who can help train their latest language model on professional document, spreadsheet, and slide deck tasks. We're looking for clinical research scientists 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
Create, evaluate, and refine AI-generated professional documents, spreadsheets, and slide decks for a foundational AI lab. 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
- Clinical carePreferred
- written communicationPreferred
- OrganizationPreferred
- materialsPreferred
- Attention to detailPreferred
- CommunicationPreferred
- Google CloudPreferred
- FlexiblePreferred
Other relevant skills
Identified from the job description. Confirm important requirements above.
- Clinical Research
- Biomedical Science
- Pharmaceutical Affairs
- Regulatory Affairs
- Clinical Study Reports
- Protocol Synopses
- Investigator Brochures
- Regulatory Dossier Modules
- Medical Affairs
- Publication Planning
- ICH-GCP Standards
- FDA Regulations
- EMA Regulations
- Technical Writing
- Spreadsheet Craftsmanship
- Slide Deck Creation
Job areas
- Science & Research
- Healthcare
- Technology
- Consulting
- Data & Analytics
Additional details
- Minimum experience
- 5+ years
- Posting language
- English
- Working hours
- 20 hours per week
- Seniority
- Mid-Senior level