Clinical Research Associate/Sr Clinical Research Associate
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Experteer Overview
As a Senior CRA, you will oversee clinical trial monitoring to ensure protocol adherence, regulatory compliance, and high data quality. You will lead monitoring activities, visit sites, and support trial execution while collaborating with cross-functional teams.Your role includes training site staff and maintaining strong relationships with site personnel to sustain smooth operations. This is a home-based role in Spain with significant travel, offering opportunities to influence trial conduct and drive continuous improvement.
You will work in a diverse, performance-driven culture that values inclusion and scientific excellence.
Compensaciones / Beneficios- Monitor study sites for protocol compliance, regulatory adherence, and GCP standards
- Conduct site visits to assess performance, resolve issues, and support trial execution
- Collaborate with cross-functional teams to ensure timely, accurate data collection and reporting
- Provide training and guidance to site staff and other CRAs to uphold high trial conduct standards
- Build and maintain effective relationships with site personnel and stakeholders to enable smooth operations
- Bachelor in a relevant scientific discipline
- Extensive experience as a Clinical Research Associate with strong understanding of trial processes and regulatory requirements
- Proven ability to manage multiple sites and projects with strong organizational and problem-solving skills
- Expertise in monitoring practices, data integrity, and site management with proficiency in relevant trial software and tools
- Excellent communication, interpersonal, and stakeholder management skills with ability to influence and drive compliance
- Willingness to travel approximately 60%
- Various annual leave entitlements
- Health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme, LifeWorks
- Life assurance
- Flexible country-specific optional benefits
Icon Clinical PLCMadrid
Experteer Overview
As a Clinical Research Associate II, you drive the conduct and oversight of clinical trials across sites. You will monitor study activities, ensure adherence to protocols and patient safety, and collaborate with investigators to...
Icon Clinical PLCMadrid
Research Associate with strong understanding of trial processes and regulatory requirements
• Ability to manage multiple sites and projects simultaneously with strong organizational and problem-solving skills
• Expertise in monitoring practices, data...
Icon Clinical PLCMadrid
Experteer Overview
As a Clinical Research Associate II at ICON, you will support the design, execution, and oversight of clinical trials to advance innovative therapies. You will ensure protocol adherence, data integrity, and patient safety while...