Senior Clinical Research Associate at ICON will oversee clinical trial monitoring activities across multiple sites in Spain, ensuring protocol adherence, regulatory compliance, and data integrity. The role involves site visits, staff training, and cross-functional collaboration in a sponsor-dedicated model.
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
- Train site staff and other CRAs to maintain high standards of trial conduct
- Build and maintain effective relationships with site personnel and stakeholders
Requirements
- Bachelor's degree in scientific or healthcare-related discipline
- Extensive experience as Clinical Research Associate with deep knowledge of trial processes
- Proven ability to manage multiple sites and projects concurrently
- Expertise in monitoring practices, data integrity, and clinical trial software
- Strong communication and stakeholder management skills
- Willingness to travel approximately 60% of the time
- Legal right to work in Spain
📌 Senior Clinical Research Associate (España)
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📍 España