SeniorProjectManager-Oncology

## Accountabilities Lead end-to-end delivery of oncology clinical trials from start-up through closeout, ensuring adherence to scope, timelines, budget, and quality standards in a regulated CRO environment. Direct cross-functional project teams, coordinating clinical operations, scientific stakeholders, and functional leads to ensure seamless execution across all trial phases. Manage financial performance, including project budgeting, forecasting, and cost control, while ensuring profitability and alignment with contractual obligations. Serve as the primary client interface, managing expectations, providing progress updates, and resolving escalations or delivery challenges proactively. Oversee risk identification and mitigation strategies, ensuring issues are addressed quickly and effectively to maintain study continuity. Ensure all project deliverables meet regulatory, operational, and sponsor requirements while maintaining high standards of quality and compliance. Requirements: This role requires strong experience in clinical project management within a CRO environment, particularly in oncology studies, combined with the ability to lead complex, multi-stakeholder programs. Candidates should bring both operational discipline and strong communication skills to manage global teams and client relationships effectively. 6–7+ years of industry experience, including at least 5 years in clinical project management within a CRO setting, with proven oncology study experience. Strong understanding of clinical trial lifecycle management, project planning, budgeting, and operational delivery in regulated environments. Demonstrated ability to lead multidisciplinary teams and manage multiple concurrent clinical projects. Excellent communication and stakeholder management skills, with the ability to translate complex clinical and operational topics for diverse audiences. Proficiency in MS Office and familiarity with clinical project management tools and systems. University degree