Teams at Jade Biosciences, Inc.

Lead strategic and operational execution of clinical trials from FIH to global Phase 3. Manage CRO/vendor selection and budgets, provide technical input to clinical documents, mitigate risk, mentor junior staff, build cross-functional relationships, and contribute to corporate materials and Clinical Operations function development.

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 pharmacovigilance strategy, safety science, regulatory reporting, vendor oversight, quality systems, inspection readiness, and cross-functional safety activities across a biotechnology portfolio. Build a scalable, inspection-ready PV function; oversee outsourced case processing and safety databases; manage SDEAs, budgets, metrics, audits, and compliance; author and review safety deliverables; and hire and develop PV personnel as the organization advances through global development.