Ergomed is seeking a Regulatory Start-Up Specialist to lead and coordinate all regulatory activities ensuring site initiation readiness for multi-country trials. You will ensure compliance with ICH-GCP and country-specific requirements, manage essential documents, and support risk management and strategic input across internal and external stakeholders. You will contribute to drafting and finalizing regulatory and site-level agreements, translating documents as needed, and maintaining timelines
📌 Global Study Start-Up (Madrid)
🏢 Ergomed
📍 Madrid
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