Teams at Jade Biosciences, Inc.

Lead GMP Quality Assurance activities for outsourced manufacturing and supply operations across clinical and commercial stages. Oversee CDMOs, review and approve quality records, manage quality agreements, drive risk management, support regulatory submissions and inspections, and coordinate cross-functional QA documentation, batch release, and issue resolution to ensure compliance with cGMP and regulatory requirements.

Provide high-level administrative support to the Chief Legal Officer and other executives: manage complex calendars, travel, and stakeholder communications; upload board materials to Boardvantage; coordinate legal document execution, board minutes, and confidential records; assist compliance tracking and audits; support cross-functional projects, process improvements, and manage department budgets, invoices, POs, and vendor relationships.

Lead clinical strategy and execution for Phase 2/3 nephrology trials. Draft and review protocols and study documents, provide medical monitoring and data review, collaborate with operations, biostatistics, regulatory and safety teams, support regulatory submissions, and contribute to scientific communications and investigator interactions.