Experteer Overview As an Associate Project Manager at ICON, you will help coordinate and manage clinical trials within a sponsor-dedicated model, contributing to study design, analysis, and advancement of therapies. You work across cross-functional teams to meet milestones and deliverables, supporting regulatory submissions and data-driven decision making. The role offers exposure to global sponsors and a collaborative culture that prioritizes patient impact and career development. You will develop and mentor teams while handling multiple priorities in a fast-paced environment. Compensaciones / Beneficios • Assist project managers in planning, execution, and monitoring of clinical trials • Coordinate study activities such as site selection, patient recruitment, and data collection • Support development of study protocols, case report forms,



and related study documents • Participate in data analysis and interpretation to aid decision-making and submissions • Collaborate with cross-functional teams to ensure milestones and deliverables are met Responsabilidades • Bachelor in relevant scientific discipline or healthcare-related field • Minimum of 2 years of experience in clinical research or project management • Strong organizational and multitasking skills • Excellent communication and interpersonal skills • Ability to work effectively in a fast-paced, team-oriented environment • Willingness to travel approximately 10% Requisitos principales • Various annual leave entitlements • Health insurance offerings • Competitive retirement planning offerings • General Employee Assistance Programme LifeWorks • Life assurance • Flexible country-specific optional benefits

📌 Associate Project Manager (Comunidad de Madrid)
🏢 Icon Clinical
📍 Comunidad de Madrid