Clinical Project Manager - Oncology (Client Dedicated/Remote)

Job Responsibilities

• Sponsor Dedicated | Remote - United States
• Are you passionate about advancing cancer research and bringing innovative therapies to patients worldwide?
• We are seeking experienced Clinical Project Managers with strong global oncology clinical trial experience to join a high-performing sponsor-dedicated team supporting a diverse portfolio of oncology studies across multiple indications and phases of development.
• This is a fully remote, US-based opportunity where you will play a critical role in the operational leadership and execution of global clinical trials.
• We are specifically seeking professionals with 3+ years of hands-on Clinical Project Management experience leading global oncology studies and collaborating with cross-functional teams, vendors, and international stakeholders.
• What You'll Do:
• As a Clinical Project Manager II, you will help drive the operational execution and delivery of global oncology clinical trials, ensuring studies are conducted efficiently, compliantly, and according to established timelines.
• Key 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
• Cook up study timelines, deliverables, risks, and issue resolution
• 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

Required Qualifications

• 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 independently and manage multiple tasks simultaneously