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Clinical & Biomedical Specialist / Pharma Consultant

Ethos Β· 100% remote Β· Contract Β· Posted

Pay
$100/hr
Location
Worldwide
Languages
English
Hours
Flexible, 5-20 hours per week
Openings
Not listed
Level
Expert

Summary

Create, evaluate, and refine AI-generated clinical and biomedical documents, spreadsheets, and slide decks for training a language model, drawing on pharmaceutical and regulatory expertise.

What you'll do

  • Create AI-generated documents, spreadsheets, and slide decks
  • Evaluate and refine AI-generated clinical and regulatory materials
  • Cover workflows such as clinical study reports, protocol synopses, investigator brochures, regulatory dossiers, and medical affairs slides

Requirements

  • Have 5+ years in clinical research, biomedical science, or pharmaceutical/regulatory affairs
  • Author or review clinical study reports, protocol synopses, or regulatory dossier modules
  • Be familiar with ICH-GCP standards and FDA/EMA regulatory expectations
  • Show expert-level document, spreadsheet, and slide craftsmanship

Skills

  • Clinical Research
  • Pharmaceutical Regulatory Affairs
  • ICH-GCP
  • FDA/EMA Regulations
  • Medical Writing
  • Document Design
  • Spreadsheets

Full description

We're working with a leading foundational AI lab to find experienced clinical and biomedical specialists who can help train their latest language model on professional document, spreadsheet, and slide deck tasks.
We're looking for pharma and clinical development professionals 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.

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