Sr. Clinical Project Manager

Role: Senior Clinical Project Manager serving as the sponsor operational lead for international clinical trials in oncology, focusing on radiopharmaceuticals and late-stage therapies. Responsibilities: lead cross-functional teams across Clinical Operations, Medical, Regulatory, Data Management, and external vendors; oversee CRO/vendor performance, study planning, site activation, enrollment, and compliance; manage budgets, timelines, risks, and study documentation; ensure quality, regulatory adherence, and study integrity; facilitate communication with internal and external stakeholders and represent Clinical Operations in meetings and audits. Qualifications: bachelor's in life sciences, PMP preferred; 5+ years in clinical trial project management, with experience in late-phase (Ph3-4), oncology, or radiopharmaceuticals; strong knowledge of ICH-GCP, regulatory processes, and global trial management; excellent communication, organizational, and leadership skills. High-Value: oncology/radiopharmaceutical focus, late clinical stage, global trial oversight, vendor management, cross-regional feasibility, and regulatory submissions. Work Setup: hybrid or remote, with international scope.