Experteer Overview In this role, you drive site engagement to support efficient clinical trials and ensure compliant study conduct. You will collaborate with trial sites and internal teams to tailor engagement strategies, monitor performance, and foster strong, compliant relationships. The position offers impact across multiple studies and sites, contributing to ICON’s mission to bring new medicines to patients faster. You will work in a values-driven environment that prioritizes integrity, collaboration, agility, and inclusion.Compensaciones / BeneficiosBuild and maintain relationships with key trial-site stakeholders (PI, site coordinators, research staff)Provide guidance on study protocols, procedures,



and regulatory requirements to site staffIdentify opportunities to improve site engagement and optimize site performanceCollaborate with internal teams to develop and implement site engagement strategies per study/site needsMonitor site performance metrics and report engagement outcomes to study teamsSupport delivery of clinical research activities with accountability for deliverablesResponsabilidadesBachelor's degree in life sciences or related fieldPrevious experience in clinical research, site management, or related field (preferred)Strong interpersonal and communication skills to build rapport with diverse stakeholdersExcellent organizational and problem-solving abilities with multitasking capacityKnowledge of ICH-GCP guidelines and regulatory requirements for clinical trialsWillingness to travel approximately 60%Eligibility to work legally in the country of the roleRequisitos principalesCompetitive base salaryPerformance-related incentivesHealth and wellbeing programmes (medical, dental, vision)Retirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resources
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📌 Site Engagment Liason (Barcelona)
🏢 Icon Clinical
📍 Barcelona