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Expert - Medical Affairs Director

Job in Indianapolis, Hamilton County, Indiana, 46262, USA
Listing for: Ethos
Part Time position
Listed on 2026-08-28
Job specializations:
  • Science
    Medical Science Liaison
Salary/Wage Range or Industry Benchmark: 100 USD Hourly USD 100.00 HOUR
Job Description & How to Apply Below
Position: Expert Opportunity - Medical Affairs Director ($100/hr, up to $2,000/week)
Location: Indianapolis

About This Opportunity

We're working with a leading foundational AI lab to find experienced medical affairs directors who can help train their latest language model on professional document, spreadsheet, and slide deck tasks.

We're looking for medical affairs directors 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/Soft Bank/Deep Mind 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
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