Clinical Site Associate
ICON · Sao Paulo, Brazil
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
This hybrid clinical research position involves coordinating and administering clinical trials while ensuring regulatory compliance. Responsibilities include managing trial documentation, supporting study materials, and tracking key metrics. The ideal candidate holds a bachelor's degree in a science or healthcare field with prior clinical research experience and knowledge of trial processes and regulations.
Privacy & handoff
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