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 / Incentivos * 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

📌 Project Director (Valencia)
🏢 Precision For Medicine
📍 Valencia