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ICON is seeking a Site Management Associate I in Brazil to support clinical trial site management and ensure compliance with study protocols. The role involves administrative and logistical support, as well as collaboration with cross-functional teams to enhance operational efficiency.
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Job Summary
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.
In addition to your competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.
Matching Summary
Match Score: 75
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ICON is seeking a Site Management Associate I in Brazil to support clinical trial site management and ensure compliance with study protocols. The role involves administrative and logistical support, as well as collaboration with cross-functional teams to enhance operational efficiency.
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Skills & Requirements
Must-have
Site monitoring activities
Adherence to study protocols
Good Clinical Practice (GCP) guidelines
Accurate record keeping
Nice-to-have
Fostering an inclusive environment
Driving innovation and excellence
Nurturing talent
Key Requirements
Bachelor’s degree in life sciences, healthcare administration, or clinical research
Global experience in clinical research, site management, or related administrative roles is preferred