Roche seeks a Clinical Site Manager specialising in IVDR and Study Start-Up to design, plan, coordinate, and conduct all activities for initiating, monitoring, and completing clinical studies at assigned sites. You will ensure studies are delivered, recorded, and reported per protocols and general regulatory guidelines.
The role involves leading site activation, submissions, and CRO oversight, working with cross-functional teams to ensure compliance and quality across regulatory submissions and
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📌 Clinical Study Start-Up Lead | Site Activation & IVDR (Madrid)
🏢 F. Hoffmann-La Roche
📍 Madrid
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