Experteer Overview
In this role you support the design and execution of clinical trials, ensuring quality data and patient safety. You’ll work with investigators and site staff to maintain compliant trial conduct and contribute to study documentation. The position offers exposure to general trials, cross-functional collaboration, and a meaningful impact on advancing therapies. This opportunity suits a detail-oriented professional who thrives in a fast-paced, international environment.

Compensaciones / Beneficios
• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensure protocol compliance, data integrity, and patient safety throughout the 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 the preparation and review of study documentation, including protocols and clinical study reports





Responsabilidades
• Bachelor's degree in a scientific or healthcare-related field
• Minimum of 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 a fast-paced environment
• Ability to travel at least 60% of the time (international and domestic) and possess a valid driver's license
• Good level of English

Requisitos principales
• Various annual leave entitlements
• Health insurance offerings
• Competitive retirement planning offerings
• Global Employee Assistance Programme (LifeWorks)
• Life assurance
• Flexible country-specific optional benefits

📌 Clinical Research Associate II (Madrid)
🏢 Icon Clinical
📍 Madrid