Experteer Overview In this role, you will oversee the conduct of clinical studies at investigational sites to ensure quality and compliance. You perform monitoring visits (on-site or remote) to confirm site readiness and ongoing suitability for the study. You verify investigators’ qualifications, resources, facilities, equipment, and staff, and you train site personnel as needed. When applicable, you support regulatory submissions to advance study approvals and timelines.Compensaciones / Incentivos
- Conduct monitoring visits (on-site or remote) to ensure site adequacy for study conduct
- Identify investigators and verify qualifications, resources, facilities, equipment, and staff
- Train investigational site staff as necessary
- Support preparation of regulatory submissions or EC submissions when applicableResponsabilidades
- Travel—national
- Experience in clinical study monitoring or site management
- Ability to assess site qualifications and capabilities
- Training and coaching of site staff
- Support for regulatory submission activitiesRequisitos principales
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📌 Clinical Research Associate Ii / Senior Cra (Madrid)
🏢 Ergomed Group
📍 Madrid