Clinical Research Associate II role at ICON involving design and analysis of clinical trials with focus on monitoring activities, data integrity, and protocol compliance. The position works within a sponsor-dedicated model supporting integral clinical trial operations. 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 resolution of 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 of experience as a 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

📌 Clinical Research Associate 2 (España)
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📍 España