SeniorProjectManager-Oncology

## Accountabilities Lead the end-to-end management of oncology clinical trials from start-up through closeout, ensuring delivery against scope, timeline, budget, and quality expectations. Coordinate cross-functional project teams and functional area leads to ensure alignment on study objectives, operational execution, and risk mitigation strategies. Oversee financial, operational, and technical aspects of assigned clinical trials, including budget tracking, forecasting, and resource planning. Ensure study deliverables comply with contractual requirements, regulatory standards, and sponsor expectations. Identify, escalate, and resolve project risks and operational issues, ensuring timely decision-making and implementation of corrective actions. Collaborate closely with scientific, clinical, and operational stakeholders to support effective study execution and data integrity. Maintain clear and consistent communication with internal teams and clients to ensure transparency and alignment throughout the study lifecycle. Requirements: 6–7+ years of experience in the clinical research industry, including at least 5 years in clinical project management within a CRO environment. Proven experience managing oncology clinical trials is required. Bachelor’s degree in Life Sciences or a related field preferred. Strong knowledge of clinical trial project management processes, including budget development and operational oversight. Demonstrated ability to lead multidisciplinary teams in complex, global clinical environments. Excellent communication skills with the ability to engage effectively with internal stakeholders and external sponsors. Strong problem-solving skills and ability to perform under pressure in fast-paced, deadline-driven environments. Proficiency in MS Office and familiarity with clinical research systems and tools. Willingness to travel as required to support study needs. Benefits: Competitive salary range aligned with experience and market standards Comprehens