09 nov
|
Medpace
|
España
Medpace is seeking a Regulatory Submissions Coordinator in Madrid, Spain, to join our Clinical Operations team. This office-based role focuses on preparing, reviewing, and filing regulatory submissions to Ethics Committees and Regulatory Agencies, while ensuring compliance with applicable guidelines.
Fluency in Spanish and English is required, and prior CRO/pharma experience is preferred. You will maintain essential documents, support queries, and help keep the clinical trial management system
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📌 Madrid: Regulatory Submissions Coordinator, Clinical Trials (España)
🏢 Medpace
📍 España