Associate Director, Clinical Site Budgets & Payments
You will architect and lead Jade Biosciences' global approach to clinical trial site budgeting, investigator grant strategy, and payment governance. This high-visibility role defines global grant philosophies, ensures compliance with FMV and transparency regulations, and oversees CRO performance for site budgets and payments across all clinical studies.
Remote|Director|Full-time|Biotechnology
Executive Director, Clinical Quality Assurance
You will lead clinical quality assurance for a clinical-stage biotech, ensuring GCP, GPvP, and GLP compliance across clinical trials. You'll act as a strategic partner to clinical teams, oversee audits, manage CAPAs, and drive inspection readiness.
Director|Full-time|Biotechnology
Senior Director, Clinical Operations
Boston, Massachusetts, United States | Chicago, Illinois, United States | San Francisco, California, United States | Seattle, Washington, United States
You'll direct the strategy and execution of clinical programs at **Jade Biosciences**, a clinical-stage biotech. You'll manage CROs, budgets, and cross-functional teams to **deliver best-in-class therapies** for autoimmune diseases. This role offers **remote flexibility** with significant leadership impact in a growing company.
Remote|Director|Full-time|Biotech
Director, GMP Quality Assurance
Boston, Massachusetts, United States | Chicago, Illinois, United States | San Francisco, California, United States | Seattle, Washington, United States
You'll lead **GMP quality oversight** for a **clinical-stage biotech** developing best-in-class autoimmune therapies. Your core impact is ensuring **compliant manufacturing and product quality** across CMOs and internal teams. This fully remote role offers the chance to shape quality strategy from Phase 1 through commercial.
Remote|Director|Full-time|Biotech
Senior/Executive Director, Quality Management System
Boston, Massachusetts, United States | Chicago, Illinois, United States | San Francisco, California, United States | Seattle, Washington, United States
You'll lead the **development and implementation** of a phase-appropriate GxP Quality Management System for **a clinical-stage biotechnology company**. Your work will ensure regulatory compliance and inspection readiness across all programs, driving **continuous improvement** in quality processes.