Overview¿Es usted el candidato adecuado para esta ocasión? Asegúrese de leer la descripción completa a continuación.In this role, you will design and analyse clinical trials and monitor sites to ensure data quality and patient safety. You will work with investigators and site staff to keep studies on track and compliant with protocols and ICH-GCP. You contribute to study documentation and data review while operating in a fast-paced, collaborative environment. You will travel up to ~60% to support global trial activities and deliver quality trial outcomes.Compensaciones / BeneficiosCompetitive base salary and performance related incentivesHealth and wellbeing programmes including medical, dental, and vision coverageRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysResponsabilidadesConduct site qualification, initiation, monitoring,



and close-out visitsEnsure protocol compliance, data integrity, and patient safetyCollaborate 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 (protocols, CSRs)Requisitos principalesBachelor in Science or Healthcare-related fieldMinimum 2 years of Clinical Research Associate experience xhfqzwm In-depth knowledge of clinical trial processes, regulations, and ICH-GCPStrong organizational and communication skills with attention to detailAbility to work independently and collaboratively in a fast-paced environmentWillingness to travel ~60%strong organizational skillseffective communicationattention to detailclinical trial processesICH-GCP guidelinesdata review and query resolution

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