Sr. Clinical Trial Manager

Role: Senior Clinical Trial Manager overseeing Phase I–III clinical studies for radiopharmaceutical therapies targeting solid tumors in oncology. Responsibilities include planning, executing, and closing trials, managing CROs and vendors, ensuring compliance with GCP/ICH/FDA regulations, monitoring progress, and mitigating risks. The role requires leading cross-functional teams, managing budgets, and participating in site feasibility and startup activities. Qualifications: 5-7 years of experience in clinical operations within biotech, pharma, or CROs, with a BA/BS in a scientific or healthcare field; expertise in clinical trial management, vendor oversight, and regulatory compliance. High-Value: Oncology, radiopharmaceutical modality, Phase I–III, regulatory compliance, CRO/vendor management, and cross-functional collaboration. Work setup: Remote in the US, with up to 20% travel.