Clinical Research Associate II position in Barcelona supporting sponsor-dedicated clinical trials. The role involves monitoring activities, ensuring protocol compliance, managing data integrity, and collaborating with site staff to advance innovative treatments. Responsibilities Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials Ensure protocol compliance, data integrity, and patient safety throughout trial process Collaborate with investigators and site staff to facilitate smooth study conduct Perform data review and resolve queries to maintain high-quality clinical data Contribute to preparation and review of study documentation including protocols and reports Requirements Bachelor's degree in scientific or healthcare-related field Minimum 2 years experience as Clinical Research Associate In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines Strong organizational and communication skills with attention to detail Ability to work independently and collaboratively in fast-paced environment Willingness to travel approximately 60% as required Legal right to work in Spain

📌 Research Associate (España)
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📍 España