Senior Clinical Project Manager (Oncology & Radioligand Therapy)
Company Overview
Our client is a premier, mid-sized Contract Research Organization (CRO) specializing in high-stakes oncology drug development. Known for their agility and deep scientific expertise, they are a leader in the rapidly evolving field of Radioligand Therapy (RLT) and targeted alphas. They offer the global reach of a large firm with the boutique, high-touch service model that allows Project Managers to truly "own" their programs.
Position Summary
The Senior Clinical Project Manager (CPM) will lead complex, global oncology programs, with a particular focus on Radioligand Therapies (RLT). This role requires a unique blend of traditional oncology trial management and the specialized logistics required for radiopharmaceuticals (e.g., supply chain coordination, site nuclear medicine readiness, and specialized safety monitoring).
Key Responsibilities
• RLT Program Leadership: Oversee the unique operational requirements of Radioligand studies, including coordinating the tight "just-in-time" delivery window for radioactive isotopes.
• Global Trial Execution: Drive the end-to-end delivery of Phase I-III global oncology trials, ensuring data integrity and milestone achievement across multiple continents.
• Sponsor Management: Act as the primary strategic partner for biotech and pharma sponsors, providing high-level transparency and proactive problem-solving.
• Site & Vendor Synergy: Manage specialized vendors (e.g., central imaging, nuclear pharmacies, and logistics providers) to ensure seamless site support.
• Financial Stewardship: Full P&L responsibility for assigned projects, including budget tracking, forecasting, and managing out-of-scope activities.
• Regulatory & Safety Compliance: Ensure strict adherence to ICH-GCP and global regulatory requirements, with specific attention to radiation safety protocols.
Required Qualifications
• Education: Bachelor’s degree in Life Sciences, Nuclear Medicine, or related field (Advanced degree preferred).
• Experience: 7+ years of clinical project management experience in Oncology.
• Specialized Knowledge: Direct experience or strong foundational knowledge in Radioligand Therapy (RLT) or radiopharmaceuticals is highly preferred.
• Global Expertise: Proven success managing trials across North America, Europe, and/or APAC.
• CRO Background: Prior experience working in a mid-sized CRO, demonstrating the ability to be both a strategic lead and a hands-on contributor.