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Overview In this role you drive and oversee multi-site oncology trials within a global program, acting as the primary client liaison and ensuring study delivery meets scope, quality, and budget goals. You’ll lead cross-functional teams, shape trial strategy, and support business objectives through process improvement and proactive risk management. The position offers remote work across EU/UK regions and opportunities to influence senior leadership and bid defense efforts. You will partner with clients and internal teams to deliver high-impact oncology programs. Compensaciones / Beneficios • fully remote work, • work-life balance, • supportive and collaborative environment, • team development, • opportunity to influence senior leadership, • travel for bid defenses Responsabilidades • Serve as primary client liaison and oversee client interactions, including proposals and presentations, • Manage all aspects of clinical trials within assigned portfolios, ensuring consistency across studies, • Provide direction to project managers across study establishment, planning, execution, procurement, and closing, • Manage study budgets, identify out-of-scope work, and drive change orders, • Oversee financial health: profitability, billing, and forecasting to meet business objectives, • Develop or supervise robust project plans with timelines, risk management, and change management, • Ensure quality management for projects, including eTMF readiness and CAPA/quality improvements, • Establish and monitor trial and team progress metrics; prepare client and senior management status updates, • Lead internal and client meetings; set expectations and drive study-level strategies, • Oversee cross-functional teams for efficient trial execution; communicate protocol issues and corrective actions, • Conduct formal presentations to diverse audiences, including bid defenses, • Ensure study-specific training and compliance across functional areas, • Support business development and travel for bid defenses; drive defense preparation, • Mentor associate/project managers and participate in SOP updates, • Provide performance feedback and address project-level issues with corrective actions, • Travel domestically and internationally as required Requisitos principales • 8+ years in clinical research or equivalent experience, • 5+ years direct project management experience, • Proficient with Microsoft Office, Microsoft Project, eTMF, EDC, CTMS, • Excellent communication, interpersonal, and organizational skills, • Experience managing highly complex and global studies or portfolios, • Mastery of ICH-GCP and relevant SOPs; strong project management techniques, • Cross-functional leadership abilities and stakeholder management, • High integrity with ability to work autonomously and in teams, • Proven ability to plan, negotiate, and deliver on timelines and budgets, • strong communication, • leadership and mentoring, • cross-functional collaboration, • Microsoft Office (Outlook, Word, Excel, PowerPoint), • Microsoft Project, • eTMF