Clinical Research Associate II position based in Madrid, Spain, responsible for monitoring clinical trials, ensuring protocol compliance, and maintaining data integrity. The role involves site visits, investigator collaboration, and documentation review within a sponsor-dedicated model at a integral contract research organization.
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
- Prepare and review study documentation including protocols and clinical study reports

Requirements
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years of clinical research associate experience
- 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 II (España)
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📍 España