Global Study Associate

Join ICON plc as a Global Study Associate in Peru, Lima, and 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.

Requirements

• Assist in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
• Support site management activities, including documentation preparation, data entry, and tracking site performance metrics.
• Collaborate with cross-functional teams to facilitate communication and address site-related issues effectively.
• Maintain accurate records of site activities and contribute to the preparation of monitoring reports.
• Participate in training and development initiatives to enhance knowledge and skills in clinical trial management.

Benefits

• Annual leave entitlements
• Health insurance offerings
• Competitive retirement planning
• Global Employee Assistance Programme
• Life assurance
• Flexible country-specific optional benefits