A leading pharmaceutical company is seeking a Clinical Trial Documentation & Records Management Lead in Parma, Italy. This role involves establishing and improving the documentation unit, ensuring compliance with regulatory standards. Ideal candidates will have 8-10 years of clinical operations experience, strong leadership skills, and knowledge of eTMF and CTMS systems. Flexible hybrid working arrangements are available. The company promotes continuous training and a supportive working environment with a focus on work-life balance.
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