Hybrid Lead: Clinical Trial Documentation

2 giorni fa


Parma, Italia Chiesi Farmaceutici S.P.A. A tempo pieno

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.#J-18808-Ljbffr



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  • parma, Italia Chiesi Farmaceutici S.P.A. A tempo pieno

    Select how often (in days) to receive an alert :Clinical Trial Documentation & Records Management LeadDepartment : Global Clinical DevelopmentBusiness Area : R&D, Pharmacovigilance & Regulatory AffairsJob Type : Direct EmployeeContract Type : PermanentLocation : Parma, ITAbout usBased in Parma, Italy, Chiesi is an international research-focused...


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