Clinical Research Associate II role at ICON involving clinical trial monitoring, site management, and data integrity oversight. Reports to sponsor-dedicated model with integral support across multiple therapeutic areas in non-oncology specialties.

Responsibilities

- Conduct site qualification, initiation, monitoring, and close-out visits
- Ensure protocol compliance, data integrity, and patient safety throughout trials
- Collaborate with investigators and site staff on study conduct
- Review clinical data and resolve data queries to maintain quality standards
- Prepare and review study documentation including protocols and reports

Requirements

- Bachelor's degree in scientific or healthcare-related field
- 3–4 years clinical trial monitoring experience at CRO or pharmaceutical company
- Comprehensive knowledge of clinical trial processes, ICH-GCP regulations
- Strong organizational, communication, and attention-to-detail skills
- Ability to work independently and collaboratively in fast-paced settings
- Willingness to travel approximately 60% for site visits
- Legal right to work in Spain; based in Galicia

📌 Clinical Research Associate II (España)
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📍 España