Descrizione Lavoro
A medical device company in Lucca is looking for a Senior Clinical Research Associate responsible for conducting monitoring visits in compliance with regulatory standards. Candidates need a minimum of 5 years' experience in clinical trial monitoring, with strong attention to detail and interpersonal skills. The role includes evaluating data accuracy, presenting findings, and ensuring compliance with applicable regulations. This position offers an opportunity to work in a dynamic environment with a focus on continuous improvement.
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