ICON plc is a world-leading healthcare intelligence and clinical research organization, inviting you to join its mission to shape the future of clinical development from our Madrid office. As a Study Start Up Associate II, you will drive site initiation activities, ensuring regulatory compliance and efficient start-up of trials, while collaborating with integral teams to deliver on time and quality.You will lead regulatory document preparation, submissions, and stakeholder coordination, and you
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📌 Study Start-Up Specialist II: Regulatory & Site Activation (Madrid)
🏢 Icon Clinical Research
📍 Madrid
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