Experteer 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 / Ventajas
• 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

Responsabilidades
• 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

Requisitos principales
• fully remote work
• work-life balance
• supportive and collaborative environment
• team development
• opportunity to influence senior leadership
• travel for bid defenses

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