Associate Director, Clinical Development

Role: Associate Director of Clinical Development specializing in designing and leading global clinical trials, particularly Ph1b and Phase 2/3 registrational studies, for AL Amyloidosis and related indications. Responsibilities: draft clinical trial protocols, support cross-functional and global collaborations, interpret and communicate trial data, develop scientific presentations, and identify new research opportunities. Requirements: MD, PhD, PharmD, or equivalent; extensive experience in trial design, protocol drafting, and regulatory interactions with US FDA; proven success in complex global clinical trials across all phases, especially Ph1b and Phase 2/3. Knowledge of GCP, FDA regulations, and international compliance essential. HighValue: clinical trial design, IND/BLA authoring, AL Amyloidosis, CAR-T therapies, regulatory expertise, Ph1b-3, global trials, cross-functional collaboration. WorkSetup: Los Angeles, CA.