Clinical Project Manager - Oncology (Client Dedicated/Remote)

Syneos Health is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. They are seeking an experienced Clinical Project Manager with strong global oncology clinical trial experience to lead the operational execution of global clinical trials, ensuring compliance and efficiency throughout the study lifecycle.

Responsibilities:

• Support and partner with Clinical Study Leads and cross-functional study teams on global oncology trials
• Lead day-to-day study management activities across study startup, conduct, maintenance, and closeout
• Manage study timelines, deliverables, risks, and issue resolution
• Oversee external vendors, CROs, central laboratories, imaging vendors, and specialty providers
• Coordinate Clinical Trial Team (CTT) meetings and drive action item follow-up
• Support study-level planning, forecasting, and operational strategy execution
• Monitor study performance metrics and proactively identify areas requiring intervention
• Ensure inspection readiness and compliance with applicable regulations and sponsor requirements
• Collaborate with stakeholders across Clinical Operations, Data Management, Biostatistics, Medical Monitoring, Regulatory Affairs, Safety, Supply Chain, and Quality
• Contribute to study status reporting and executive-level communications
• Support achievement of study milestones, enrollment targets, database locks, and study closeout activities

Requirements:

• Bachelor's degree in a scientific, healthcare, or related field is required
• 3+ years of Clinical Project Management experience supporting global oncology clinical trials
• Experience managing studies across multiple countries and regions (North America, Europe, Asia-Pacific, Latin America, or other global regions)
• Vendor management experience required
• Strong understanding of clinical trial operations and study lifecycle management
• Experience supporting Phase I, Phase II, Phase III, and/or Phase IV oncology studies
• Strong working knowledge of ICH-GCP guidelines and clinical research regulations
• Proficiency with Microsoft Office Suite
• Ability to work effectively within global, cross-functional matrix organizations
• Experience independently leading global oncology studies
• Experience supporting complex, multi-regional Phase II and Phase III programs
• Experience with early-phase oncology studies (Phase I/Ib)
• Experience with immuno-oncology, targeted therapies, cell therapy, or hematologic malignancies
• Familiarity with CTMS, eTMF, IRT/RTSM, and clinical data review platforms
• Experience working in sponsor-dedicated or FSP environments