Associate Director, Clinical Operations

Role: The Associate Director, Clinical Operations leads strategic planning and execution of global clinical trials in oncology, ensuring timely, compliant, and budget-conscious delivery. Responsibilities encompass developing operational strategies, overseeing trial execution, vendor and CRO management, risk mitigation, and supporting regulatory readiness. They contribute to clinical development plans and protocol design, lead cross-functional study teams, and ensure inspection preparedness. Qualifications include a BA/BS in a scientific or healthcare field, with 6-8+ years of clinical operations experience, notably in oncology and radiopharmaceuticals or theranostics preferred. Leadership or people management experience is desirable. Core skills involve strong leadership, project and resource management, deep understanding of GCP/ICH regulations, and proficiency with trial management tools like Microsoft Project or SmartSheets. The role requires up to 20% travel, with work primarily remote in the U.S. The position emphasizes collaboration with vendors, regulatory agencies, and internal teams, with a focus on high-quality trial execution in the oncology therapeutic area, including radiopharmaceutical modalities.