Site Specialist - Barcelona, Spain - office or homebased
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Site Specialist II at ICON , you will play a key role in supporting clinical trial sites in Spain , helping studies progress efficiently through start-up, activation and ongoing site management.
Working independently across assigned sites and studies, you will act as an important operational point of contact for sites and internal study teams, ensuring documentation, regulatory activities, systems and key milestones are managed accurately and in line with study requirements.
This is an excellent opportunity for someone with hands-on EU Clinical Trials Regulation (EU CTR) experience who understands the requirements of working with clinical trial sites in Spain.
What You Will Do
You will independently manage a range of site-level activities,
supporting efficient study start-up and maintenance throughout the study lifecycle.
Key responsibilities include:
- Coordinating the collection, review and maintenance of essential site documentation, ensuring completeness, accuracy and compliance with study and regulatory requirements.
- Supporting site start-up and regulatory activities in accordance with EU CTR requirements .
- Acting as a key operational contact for Spanish investigator sites, providing guidance on documentation, systems, timelines and study processes.
- Tracking site progress, milestones and outstanding actions, ensuring information is accurately maintained within relevant clinical trial management systems.
- Working closely with Site Activation, Regulatory, Clinical Operations and other cross-functional teams to identify and resolve issues that could impact site timelines.
- Supporting ongoing site maintenance activities throughout the stud
📌 Site Specialist II (España)
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📍 España