ICON plc, a leading healthcare intelligence and clinical research organization, seeks a Study Start Up Associate I in Mexico to support initiation of clinical trials and ensure regulatory compliance. You will handle site start-up activities and work with stakeholders to enable study activation.
Responsibilities include regulatory document preparation, coordinating approvals, maintaining submission records, and assisting in study document development. Travel ~5%.
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📌 Remote Study Start-Up Associate I | Regulatory Submissions (México)
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📍 México
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