Experteer Overview

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In this role, you will perform monitoring activities across pre-study to close-out phases to ensure investigational sites remain qualified and capable. You will verify investigator qualifications, resources, facilities, and staff, and you will train site staff as needed. When applicable, you will support regulatory and EC submissions. This role may be on-site or remote with national travel, contributing to study integrity and regulatory compliance. You will work closely with study teams to enable successful conduct of clinical trials and site readiness.

Compensaciones / Beneficios
• Conduct on-site or remote monitoring visits across pre-study, initiation, interim, and close-out phases
• Verify investigator qualifications, resources, xghoner facilities, equipment, and staff adequacy throughout the study
• Train investigational site staff as necessary
• Support preparation of regulatory and/or EC submissions when applicable

Responsabilidades
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Requisitos principales
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📌 Clinical Research Associate II (Madrid)
🏢 Ergomed Group
📍 Madrid