Experteer Overview In this role you will lead clinical trial start-up activities to enable timely site activation while ensuring regulatory compliance. You will work with cross-functional teams to streamline processes, guide study teams and sites, and advance start-up strategies. The position challenges you to manage multiple projects in a fast-paced environment and stay up-to-date with industry regulations. This role offers a meaningful impact on how ICON delivers efficient, compliant trials at scale.Compensaciones / Beneficios
- Lead preparation and submission of regulatory documents for approvals and site activation
- Coordinate with cross-functional teams to streamline study start-up processes
- Oversee/site identification and selection to meet project criteria and compliance
- Provide guidance and support to study teams and sites during start-up
- Stay current with regulations and trends to enhance start-up strategiesResponsabilidades




- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience in study start-up activities with regulatory knowledge
- Experience managing multiple projects and prioritizing in a fast-paced environment
- Excellent organizational skills and attention to detail
- Strong communication and interpersonal skills for collaboration with diverse stakeholders
- Commitment to high standards of quality and compliance
- Willingness to travel approximately 15%Requisitos principales
- Annual leave entitlements
- Health insurance offerings
- Competitive retirement planning
- General Employee Assistance Programme LifeWorks
- Life assurance
- Flexible country-specific benefits

📌 Clinical Trial Submission Coordinator (Madrid)
🏢 Icon Clinical
📍 Madrid