Clinical Trial Documentation & Records Lead (eTMF/CTMS)

A leading pharmaceutical company in Parma, Italy, seeks a Clinical Trial Documentation & Records Management Lead to ensure compliance with regulatory standards and manage clinical trial technologies. The ideal candidate has 8-10 years of experience in clinical operations and a robust understanding of eTMF and CTMS. This role emphasizes team leadership, cross-functional collaboration, and strategic vendor management. Join us to enhance the oversight and integrity of clinical studies while making a significant impact in the field.
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