Lavori attuali relativi a Global Clinical Quality Assurance Lead - WorkFromHome - Boston Scientific Gruppe


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    Overview A leading medical solutions company is seeking a Principal Clinical Quality Assurance Specialist to ensure clinical compliance and oversee quality assurance processes within clinical trials. The role is hybrid, requiring collaboration with global teams in the management of significant clinical device studies. Responsibilities Oversee quality...


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    A leading medical solutions company is looking for a Principal Clinical Quality Assurance Specialist to ensure compliance in clinical trials and oversee quality assurance processes. This hybrid role involves collaboration with global teams in managing significant clinical device studies across multiple sites. The ideal candidate will have extensive...


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  • WorkFromHome, Italia Chiesi Group A tempo pieno

    A global pharmaceutical company based in Parma, Italy is seeking a Clinical Trial Documentation & Records Management Lead. 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...


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  • WorkFromHome, Italia CPL & Taylor by Synergos Srl A tempo pieno

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    Select how often (in days) to receive an alert: Senior Director, Clinical Biometrics & Analytics Department: Global Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical...

Global Clinical Quality Assurance Lead

60 minuti fa


WorkFromHome, Italia Boston Scientific Gruppe A tempo pieno

Overview A leading medical solutions company is seeking a Principal Clinical Quality Assurance Specialist to ensure clinical compliance and oversee quality assurance processes within clinical trials. The role is hybrid, requiring collaboration with global teams in the management of significant clinical device studies. Responsibilities Oversee quality assurance processes within clinical trials to ensure compliance with applicable regulations and standards. Collaborate with global teams to manage significant clinical device studies across multiple sites and regions. Qualifications Extensive experience in clinical research and compliance. Strong problem-solving and communication skills. #J-18808-Ljbffr