This role coordinates clinical trial site activation and start-up activities across multiple European locations. The successful candidate will prepare regulatory submissions, manage site selection, oversee compliance, and lead cross-functional teams through the study initiation phase. The position requires clinical research experience, a scientific background, and strong organizational abilities, with approximately 15% travel expected.
Responsibilities
- Lead preparation and submission of essential documents for regulatory approvals
- Coordinate site start-up and activation delivery while resolving emerging issues
- Identify and select clinical sites meeting project criteria and compliance standards
- Provide guidance and support to study teams during the start-up phase
- Collaborate with project management,



clinical operations, and regulatory affairs teams

Requirements
- Bachelor's degree in scientific or healthcare-related field
- Extensive clinical research study start-up and site activation experience
- Strong understanding of regulatory requirements and compliance standards
- Demonstrated ability to manage multiple projects and competing priorities
- Excellent organizational skills with strong attention to detail
- Effective communication and interpersonal abilities for cross-functional collaboration
- Willingness to travel approximately 15% as required

📌 Clinical Trial Submission Coordinator (España)
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📍 España