04 sep
|
Ergomed Group
|
Madrid
04 sep
Ergomed Group
Madrid
Experteer Overview
In this role you will conduct on-site or remote monitoring activities across study phases to ensure investigational sites remain suitable for the study. You will verify investigators’ qualifications and the availability of appropriate facilities, equipment, and staff. You will train site staff as needed and, where relevant, assist with regulatory submissions. Your work supports study integrity and compliance by ensuring sites can conduct the trial to protocol and regulatory standards.
Compensaciones / Incentivos
• Conduct monitoring visits (on-site or remote) to verify site adequacy for study conduct
• Identify investigators and confirm qualification, resources, facilities, equipment, and staff for the study
• Provide training to investigational site staff as needed
• Assist in preparation of regulatory submissions (where applicable)
Responsabilidades
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Requisitos principales
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📌 Clinical Research Associate II (Madrid)
🏢 Ergomed Group
📍 Madrid