Expert Opportunity - Medical Affairs Director ($100/hr, up to $2,000/week)

About the Role

We're partnering with a leading foundational AI lab to identify experienced medical affairs directors who can help train their latest language model on professional document, spreadsheet, and slide deck tasks. The role involves creating, evaluating, and refining AI-generated documents, spreadsheets, and slide decks across core workflows such as clinical study reports, protocol synopses, investigator brochures, regulatory dossier modules, medical affairs slide decks, and publication plans.

Responsibilities

• Create, evaluate, and refine AI-generated clinical study reports, protocol synopses, and regulatory dossier modules.
• Develop and review investigator brochures and medical affairs materials with scientific rigor.
• Produce and assess medical affairs slide decks and publication plans.
• Ensure all documents meet ICH-GCP standards and FDA/EMA regulatory expectations.

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.

Qualifications

• 5+ years of experience in clinical research, biomedical science, or pharmaceutical/regulatory affairs.

Pay

$100/hour

Schedule

Flexible, 5-20 hours per week (or more if desired). Fully remote, work on your own schedule.

Start date: ASAP