Experteer Overview In this role you will lead the initiation of clinical trials, ensuring regulatory compliance and contributing to the advancement of therapies. You will drive site start-up and activation, coordinate with internal and external stakeholders, and manage regulatory submissions and documentation. You will guide study teams on regulatory requirements and best practices, and participate in process improvements to increase efficiency. This position supports ICON’s mission to shape the future of clinical development and offers cross-functional collaboration and impact across trial initiation. Compensaciones / Beneficios • Lead preparation and submission of regulatory documents (CTA, ethics submissions, regulator communications) • Coordinate with internal and external stakeholders to obtain approvals for study initiation • Maintain comprehensive records of regulatory submissions, approvals,



and correspondence • Provide guidance to study teams on regulatory requirements and best practices for start-up • Participate in process improvement initiatives to streamline start-up processes and efficiency Responsabilidades • Bachelor's degree in life sciences or related field • Minimum 2 years of experience in clinical research or regulatory affairs with study start-up experience • Strong understanding of regulatory requirements and guidelines (ICH-GCP and local) • Excellent organizational and project management skills • Excellent communication and interpersonal skills; ability to collaborate with cross-functional teams • Willingness to travel approximately 5% Requisitos principales • annual leave entitlements • health insurance offerings • retirement planning offerings • General Employee Assistance Programme LifeWorks • life assurance • flexible country-specific optional benefits

📌 Study Start Up Associate II (Madrid)
🏢 Icon Clinical
📍 Madrid