ICON plc in Reading, United Kingdom, is seeking a Clinical Quality Compliance Lead to drive quality assurance and regulatory compliance across clinical trials. You will design and analyse trial documentation, participate in audits, and collaborate with cross-functional teams to implement improvements.
The role requires a scientific background, strong regulatory knowledge (FDA/EMA/ICH-GCP/ISO), and willingness to travel up to ~65%. A competitive salary and comprehensive benefits are offered.
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