Eblex Group is supporting an innovative biotechnology company in Spain to appoint an experienced GCP Consultant to provide quality oversight across its clinical development programmes. This role focuses on ensuring studies are conducted in accordance with ICH-GCP, EU Clinical Trial Regulation, and EMA requirements, while supporting inspection readiness and quality management activities.
Join a growing biotech environment in Madrid and collaborate with Clinical Operations, Regulatory Affairs,
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📌 GCP Quality Lead for Clinical Trials | Audit (España)
🏢 Eblex Group
📍 España
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