IQVIA Biotech is seeking a Clinical Associate Submissions Representative in Italy. You will handle site activation tasks, prepare and submit regulatory documents, and ensure compliance with EUCTR/CTIS procedures while coordinating with activation managers and project teams.
The role requires EU CTR experience for Italy, local language proficiency, and strong knowledge of country requirements. Homebased in Italy with responsibilities across SA activities and regulatory deliverables.
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📌 Remote Italy Regulatory Submissions (Italia)
🏢 Altro
📍 Italia