Associate Director, Clinical Science

Role: Associate Director of Clinical Science supporting RayzeBio's radiopharmaceutical oncology programs, focusing on clinical trial development and execution. Responsibilities include designing and reviewing study protocols, managing data analysis, overseeing study start-up and closeout, contributing to regulatory documentation such as INDs and NDAs, and supporting cross-functional collaboration with Medical Writing, Clinical Operations, and regulatory teams. The role involves scientific review, problem-solving in clinical studies, and potentially leading specific project components, with a focus on radiopharmaceuticals for cancer indications. Qualifications: MS with 6+ years or BS with 8+ years of drug development experience, including at least 5 years in clinical research within biotech or pharma. Preferred: PharmD or PhD. Skills include knowledge of clinical trial design, FDA/EMA/ICH regulations, data review, and cross-functional collaboration; proficiency in Microsoft Office and data platforms like SpotFire. High-Value: Oncology, radiopharmaceutical modality, clinical trial phases (likely early to late-stage), regulatory document preparation, GxP environment. Work setup: Hybrid in Princeton, NJ, or San Diego, CA, with 20% travel.