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A global pharmaceutical company based in Parma, Italy is seeking a Clinical Trial Documentation & Records Management Lead.
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This role requires leadership in managing clinical documentation and records, ensuring compliance with regulatory standards, and overseeing clinical trial technologies.
Candidates should have 8-10 years of experience in clinical operations and leadership skills, as well as familiarity with Veeva systems.
A dynamic and supportive working environment is offered along with flexible working arrangements. xysqume
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