Senior Clinical Research Associate position at ICON in Madrid, Spain, overseeing clinical trial monitoring activities. Lead site monitoring tasks, conduct assessments, and guide cross-functional teams to ensure protocol adherence and regulatory compliance. Home-based role requiring approximately 60% travel. Responsibilities Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards Conduct site visits to assess performance, resolve issues,



and provide operational support Collaborate with cross-functional teams on timely and accurate data collection and reporting Provide training and guidance to site staff and other CRAs on trial conduct standards Build and maintain effective relationships with site personnel and stakeholders Requirements Bachelor's degree in scientific or healthcare-related discipline Extensive Clinical Research Associate experience with strong clinical trial process knowledge Ability to manage multiple sites and projects with strong organizational skills Expertise in monitoring practices, data integrity, and clinical trial software Excellent communication and stakeholder management abilities Willingness to travel approximately 60% of the time Compensation: Competitive base salary and performance-related incentives

📌 Senior Clinical Research Associate (España)
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📍 España