Overview As a Clinical Research Associate II at ICON, you will support the design, monitoring and analysis of clinical trials to advance innovative therapies. You will ensure protocol compliance, data integrity and patient safety while collaborating with investigators and site staff. Your work helps maintain high-quality data and documentation for study reports. This role offers exposure to general trials and a fast-paced, cross-functional environment that values inclusive, high-performance teams.

Compensaciones / BeneficiosAnnual leave entitlementsHealth insurance offeringsRetirement planning offeringsGlobal Employee Assistance ProgrammeLife assuranceFlexible country-specific benefits ResponsabilidadesConduct site qualification, initiation, monitoring and close-out visits for trialsEnsure protocol compliance,



data integrity and patient safety throughout the trialCollaborate with investigators and site staff to facilitate study conductPerform data review and resolve queries to maintain high-quality clinical dataContribute to preparation and review of study documentation including protocols and clinical study reports Requisitos principalesBachelor's degree in a scientific or healthcare-related fieldMinimum of 2 years of experience as a Clinical Research AssociateKnowledge of clinical trial processes, regulations and ICH-GCP guidelinesStrong organizational and communication skills, attention to detailAbility to work independently and collaboratively in a fast-paced environmentAbility to travel at least 60% of the time with a valid driver’s licenseGood level of EnglishStrong communicationAttention to detailTeam collaborationClinical trial processesICH-GCP knowledgeData query resolution

📌 CRA 2 - barcelona
🏢 Jobrapido
📍 Barcelona