Site Management Associate I – Office-based – Malaysia

ICON plc is a world‑leading healthcare intelligence and clinical research organization. We foster an inclusive environment and drive innovation in clinical development.

What You Will Do

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Key Responsibilities

• 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.
• Part...