About this role
About the Role Site Management Associate I at ICON supports management of clinical trial sites by assisting with site monitoring activities and ensuring compliance with study protocols, while maintaining high operational efficiency. What You'll Do
- Assist in monitoring clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP)
- 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 What We're Looking For
- Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research (required)
- Working experience in clinical research, site management, or related administrative support roles (preferred)
- Knowledge of clinical trial processes and regulatory requirements (a plus)
- Advanced English
- Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment
- Willingness to travel approximately 25%
- Self-motivated and able to operate in a hybrid/office-based setting in Sao Paulo, Brazil Nice to Have
- Knowledge of regulatory requirements is a plus Compensation & Benefits
- Competitive salary in USD
- Various annual leave entitlements
- Health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme (LifeWorks)
- Life assurance and optional benefits (childcare vouchers, gym discounts, subsidized travel passes, health assessments, etc.)