About This Opportunity We're collaborating with a prominent foundational AI lab seeking experienced clinical research associates to assist in training their latest language model on professional document, spreadsheet, and slide deck tasks. ## The Role You will leverage your clinical research expertise to create, evaluate, and refine AI-generated documents, spreadsheets, and slide decks across essential workflows, including clinical study reports, protocol synopses, investigator brochures, regulatory dossier modules, medical affairs slide decks, and publication plans. ## Responsibilities - Author and review clinical study reports, protocol synopses, and regulatory dossier modules for pharmaceutical, biotech, or CRO organizations. - Ensure compliance with ICH-GCP standards and FDA/EMA regulatory expectations. - Maintain scientific rigor in investigator brochures and medical affairs materials. - Demonstrate expert-level skills in document, spreadsheet, and slide craftsmanship, ensuring excellent written communication and attention to detail. ## Qualifications - Minimum of 5 years of experience in clinical research, biomedical science, or pharmaceutical/regulatory affairs. - Proven experience in authoring or reviewing relevant clinical documents. - Strong familiarity with ICH-GCP standards and regulatory expectations. ## What We Offer - Compensation: $100/hour - Flexible commitment: 5-20 hours per week (or more if desired) - Fully remote work, allowing you to set your own schedule - Immediate start date with a dynamic team at the forefront of AI development. If you're ready to make an impact in the field of clinical research, we encourage you to apply and join us in this exciting opportunity.