Descripción del trabajoExperteer Overview In this role you will lead clinical trial start-up activities to enable timely site activation while ensuring regulatory compliance. You will work with cross-functional teams to streamline processes, guide study teams and sites, and advance start-up strategies. The position challenges you to manage multiple projects in a fast-paced environment and stay up-to-date with industry regulations.

This role offers a meaningful impact on how ICON delivers efficient, compliant trials at scale.

Compensaciones / BeneficiosLead preparation and submission of regulatory documents for approvals and site activationCoordinate with cross-functional teams to streamline study start-up processesOversee/site identification and selection to meet project criteria and complianceProvide guidance and support to study teams and sites during start-upStay current with regulations and trends to enhance start-up strategiesResponsabilidadesBachelor's degree in a relevant scientific discipline or healthcare-related fieldExtensive experience in study start-up activities with regulatory knowledgeExperience managing multiple projects and prioritizing in a fast-paced environmentExcellent organizational skills and attention to detailStrong communication and interpersonal skills for collaboration with diverse stakeholdersCommitment to high standards of quality and complianceWillingness to travel approximately 15%Requisitos principalesAnnual leave entitlementsHealth insurance offeringsCompetitive retirement planningGlobal Employee Assistance Programme LifeWorksLife assuranceFlexible country-specific benefits

📌 Clinical Trial Submission Coordinator (Madrid)
🏢 Icon Clinical
📍 Madrid