Overview¿Es este el puesto que está buscando? Si es así, siga leyendo para obtener más detalles y no olvide enviar su solicitud hoy mismo.In this role you will oversee and drive the conduct of clinical trials to ensure alignment with protocol, GCP, and regulatory standards. You will monitor sites, manage data integrity, and support cross-functional teams to enable compliant, timely trial execution. You’ll train site staff, build strong relationships with stakeholders, and travel as needed to ensure successful study delivery. Join ICON’s inclusive, high-performing culture as you help shape the future of clinical development.Compensaciones / BeneficiosVarious annual leave entitlementsHealth insurance offeringsCompetitive retirement planningGlobal Employee Assistance ProgrammeLife assuranceFlexible country-specific optional benefitsResponsabilidadesMonitor clinical trial sites for protocol, GCP,



and regulatory adherenceConduct site visits to assess performance and resolve issuesCollaborate with cross-functional teams to ensure accurate data collection and reportingProvide training and guidance to site staff and other CRAsBuild and maintain relationships with site personnel and stakeholders for smooth operationsRequisitos principalesAdvanced degree in life sciences, nursing, or medicineExtensive experience as a Clinical Research AssociateAbility to manage multiple sites and projects simultaneouslyExpertise xhfqzwm in monitoring, data integrity, and site managementProficiency in relevant clinical trial software and toolsExcellent communication, interpersonal, and stakeholder management skillsAbility to travel at least 60% with a valid driver’s licenseStrong communication and interpersonal skillsStakeholder managementProblem-solving and organizational skillsMonitoring practicesData integritySite management

📌 Clinical Research Associate (Gracia)
🏢 Alira Health
📍 Gracia