Site Management Associate
ICON is a integral healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

We are currently seeking a Site Management Associate I to join our diverse and dynamic team. As a Site Management Associate I at ICON, you will play an important role in supporting the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintaining high standards of operational efficiency. You will contribute to the success of clinical research by providing essential administrative and logistical support to site management teams.
What You Will Be Doing:
Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
Supporting site management activities,



including documentation preparation, data entry, and tracking site performance metrics.
Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively.
Maintaining accurate records of site activities and contributing to the preparation of monitoring reports.
Participating in training and development initiatives to enhance knowledge and skills in clinical trial management.
Your Profile:
Bachelor’s degree in a relevant field such as life sciences, healthcare administration, or clinical research.
Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory.
Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively.
Basic knowledge of clinical trial processes and regulatory requirements is a plus.
Excellent communication and interpersonal sk

📌 SMA II (Madrid)
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📍 Madrid