Overview As Site Specialist II at ICON, you support clinical trial sites in Spain to drive start-up, activation, and ongoing site management. You act as a key operational contact for Spanish investigator sites and internal study teams, ensuring regulatory activities, documentation, and milestones are managed accurately. The role requires hands-on EU CTR knowledge and collaboration across regulatory, clinical operations, and site teams. You will identify delays, drive follow-ups, and contribute to process improvements that accelerate study timelines. This position offers meaningful work shaping site operations in a general health research context.

Compensaciones / BeneficiosCompetitive base salary and performance related incentivesHealth and wellbeing programmesRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities ResponsabilidadesCoordinate collection and maintenance of essential site documentation to ensure regulatory complianceSupport site start-up and regulatory activities per EU CTR requirementsAct as operational contact for Spanish investigator sites, guiding documentation, systems, timelines, and processesTrack site progress, milestones,



and actions within clinical trial management systemsCollaborate with Site Activation, Regulatory, Clinical Operations and cross-functional teams to resolve issues impacting timelinesSupport ongoing site maintenance throughout the study lifecycleProactively identify delays or operational challenges and drive follow-up with sites and stakeholdersContribute to process improvements and share best practicesProvide guidance and support to junior colleagues as appropriate Requisitos principalesBachelor’s degree in life sciences, healthcare or related discipline or equivalent clinical research experienceExperience in site support, site activation, start-up, regulatory, or clinical trial operations in CRO/pharma or similar environmentHands-on experience with EU CTR processesGood understanding of clinical trial documentation, GCP and site-level regulatory requirementsFluent in Spanish and English with strong communication skillsStrong organizational skills with ability to manage multiple sites and deadlinesProactive, solution-focused approach and confident working with investigator sites and cross-functional teamsproactive problem-solvingstrong communicationorganization and time managementEU CTR processesGCP and site regulatory requirementsclinical trial documentation

📌 Site Specialist II - barcelona
🏢 Jobrapido
📍 Barcelona