Senior Clinical Site Manager, Monitoring & Compliance

IQVIA is seeking a Clinical Research Associate to oversee monitoring of assigned studies, ensuring regulatory compliance and timely data capture. The role involves coordinating site activities, managing TMF/ISF documents, and liaising with the study team to support study execution.

Applicants should have a life sciences degree, at least 2 years of on-site monitoring experience, and strong knowledge of GCP/ICH guidelines, with proficient English communication and Microsoft Office skills.

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