Teams at Jade Biosciences, Inc.

Manage end-to-end document lifecycle and training programs for biotech R&D. Maintain controlled documentation, training matrices, audit-ready records, version control, and continuous improvement. Support system changes, cross-functional collaboration, and report generation for management reviews.

Lead immunology-driven translational research across pipeline programs. Design and oversee mechanism-of-action studies (in vitro/ex vivo/in vivo) with CROs, generate and interpret complex immunology datasets, prioritize indications and targets, align preclinical findings with clinical strategy, support external collaborations, author regulatory and scientific documents, and present results internally and externally.

Lead GCP compliance for clinical programs: oversee vendor and monitoring oversight, drive inspection readiness, analyze compliance metrics, manage non-compliance and CAPAs, support audits, and deliver training to ensure trials meet ICH-GCP, regulatory, and internal quality standards.