Lead strategic and operational planning of interventional oncology trials Manage global clinical studies in alignment with strategy, budget, and SOPs Collaborate on development of study materials, systems, and regulatory submissions Engage with external physicians and key opinion leaders (KOLs) Oversee clinical trial budgets (up to 25%) including forecasting and variance reviews Direct CROs and clinical vendors Ensure audit readiness and risk management throughout the study lifecycle Present study progress, data, and risks to leadership Provide clinical input to product development teams Domestic travel: 10-25% Bachelor's degree with 5+ years of oncology-related experience 1-3 years in early feasibility oncology clinical research 1-3 years of project/trial management experience 1-3 years of financial and budget management experience Experience working with CROs and clinical vendors Experience in solid tumor, medical device, or drug development Familiarity with product development teams Innovative thinking and problem-solving Strategic execution with minimal supervision Strong collaboration and influence across global stakeholders Adaptability in dynamic and uncertain environments