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information • Experience in leading cross-functional, multi-cultural teams • Experience with (safety or others) issue management • Experience in drug development, clinical trial methodology, regulatory
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projects/products and be an active member of the Global Program Team (GPT), Global Clinical Team (GCT) and Clinical Trial Team (CTT). • Is responsible for safety issue management from formation of Global
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reports on trial data for use of safety and clinical boards (e.g., Safety Management Team, Global Clinical Team, Global Program Team) with appropriate oversight from the Medical Lead • Providing input
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expertise and leadership and drive success of early global programs (Ph1 and Ph2a) • Responsible for clinical monitoring and integrated safety data review during and after the live phase of a study. • Drive
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the program after Proof of Concept by delivering key Profiling data to support regulatory submissions • Recognized Expert in field, drives project team clinical strategy. Works globally across Novartis as
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member of the Global Program Team (GPT), Global Clinical Team (GCT) and Clinical Trial Team (CTT) • Developing, and overall responsibility for key internal Novartis safety documents: reviewing
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Primary Location: Barcelona, Spain (hybrid) Alternate Location: United Kingdom (remote) About this role: As our Global Program Safety Lead within the CRM therapeutic area you will provide scientific
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safety input to the clinical development program for assigned projects/products, participating as an active member of the Global Program Team (GPT), Global Clinical Team (GCT) and Clinical Trial Team (CTT
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Job Purpose In close collaboration with the Global Program Safety Lead (GPSL) provides robust safety evaluation expertise and medical innovation in order to improve patients’ lives and impact on
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significantly impacts the entire Novartis Neurodegenerative drug development pipeline. In this key position you will: • Drive success of early global programs, develop and implement strategies to achieve clinical