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

About the Role

We're partnering with a leading foundational AI lab to identify experienced directors of clinical development 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 assess investigator brochures, medical affairs slide decks, and publication plans.
• Ensure adherence to ICH-GCP standards, FDA/EMA regulatory expectations, and scientific rigor.

Requirements

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

Pay

$100/hour

Schedule

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