Experteer Overview
In this role you will oversee clinical trial activities to ensure protocol, regulatory, and GCP compliance.

You will lead site monitoring with a focus on quality and continuous improvement, support cross-functional data collection and reporting, and train site staff and CRAs.

You will build strong relationships with site personnel to enable smooth trial operations, and you will travel as needed to managed sites.

This role offers an opportunity to shape trial execution within a integral, inclusive environment that values excellence.

Compensaciones / Beneficios
• Monitor sites to ensure adherence to study protocols, regulatory requirements, and GCP standards
• Perform site visits to assess performance, resolve issues and support trial execution
• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting
• Provide training and guidance to site staff and other CRAs to maintain high standards




• Build and maintain relationships with site personnel and stakeholders to facilitate smooth operations

Responsabilidades
• Bachelor in a relevant scientific discipline or healthcare-related field
• 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; proficiency in relevant clinical trial software and tools
• Excellent communication, interpersonal, and stakeholder management skills; ability to drive compliance in a complex environment
• Willingness to travel approximately 60%

Requisitos principales
• competitive salary
• annual leave entitlements
• health insurance offerings
• retirement planning options
• Global Employee Assistance Programme Life

Works
• life assurance

📌 CRA III / CRA II (España)
🏢 Icon Clinical
📍 España