Found Description
Temporary role - CTC Logistics - Chile
As a SMA I at ICON, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintaining high standards of operational efficiency.
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.
- Participating in training and development initiatives to enhance knowledge and skills in clinical trial management.