Clinical Project Manager - Oncology (Client Dedicated/Remote)

Job 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 Clinical Trial Team (CTT) meetings and drive action item follow-up
• Support study-level planning, forecasting, and operational strategy execution
• Maintain 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
• 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
• Able to work effectively within global, cross-functional matrix organizations
• Oncology Therapeutic Area Experience

Preferred Qualifications

• 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)
• Familiarity with CTMS, eTMF, IRT/RTSM, and clinical data review platforms
• Experience working in sponsor-dedicated or FSP environments

Key Skills & Competencies

• Strong project management and organizational skills
• Excellent communication and stakeholder management abilities
• Prominent risk identification and mitigation capabilities
• Detail-oriented with a focus on quality, compliance, and execution
• Strong collaboration skills across global teams and functions
• Influence without direct authority and drive accountability across study teams

Additional Information

The Company, at its sole discretion, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above.