ICON seeks a Clinical Research Coordinator for a part-time position in Valencia, Spain to oversee day-to-day clinical trial operations, manage participant recruitment and site logistics, and ensure compliance with study protocols and regulatory standards.

Responsibilities

- Coordinate operational aspects of clinical trials including recruitment, scheduling, and site logistics
- Ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards
- Monitor trial progress and document data collection, safety reporting, and regulatory compliance
- Provide training and support to site staff on trial procedures and protocols
- Build relationships with study participants and site personnel to facilitate trial operations

Requirements

- Bachelor's degree in scientific or healthcare-related field
- Extensive experience as Clinical Research Coordinator with knowledge of trial processes
- Strong organizational skills and ability to multitask across trial components
- Proficiency in clinical trial software and data management tools
- Excellent communication and problem-solving abilities with diverse teams

📌 Clinical Research Coordinator (España)
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📍 España