Overview

Desplácese hacia abajo para obtener una visión general completa de lo que requerirá este trabajo. ¿Es usted el candidato adecuado para esta oportunidad?

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 xqziphu 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 general 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 - Precision for Medicine (España)
🏢 Jobrapido
📍 España