Overview As a Clinical Research Associate II at ICON, you contribute to designing and analyzing clinical trials and interpreting medical data to advance innovative therapies. You will oversee site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance, data integrity, and patient safety. You will collaborate with investigators and site staff and support data review and study documentation. This role combines independent work with cross-functional teamwork to sustain trial quality and impact.

Compensaciones / BeneficiosAnnual leave entitlementsHealth insurance offeringsRetirement planning offeringsGlobal Employee Assistance Programme (TELUS Health)Life assuranceFlexible country-specific benefits ResponsabilidadesConduct site qualification, initiation, monitoring, and close-out visits for clinical trialsEnsure protocol compliance, data integrity,



and patient safety throughout the trial processCollaborate with investigators and site staff to facilitate smooth 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 AssociateIn-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelinesStrong organizational and communication skills with attention to detailAbility to work independently and collaboratively in a fast-paced environmentAbility to travel at least 60% of the time (international and domestic) and a valid driver’s licenseGood level of EnglishStrong organizational skillsEffective communicationAttention to detailIndependent and collaborative work styleKnowledge of clinical trial processes and ICH-GCP guidelinesData review and query resolution

📌 Clinical Research Associate II - Icon Clinical PLC (Barcelona)
🏢 Jobrapido
📍 Barcelona