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meetings • Safely and effectively work with radionuclides • Critical reading of the literature and ability to apply it to the project. • Closely work with multiple teams across expertise groups within
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Management Team (SMT). Ensures that this team appropriately and timely reviews all medical safety data from various sources (e.g. pre-clinical, clinical trial data post-marketing, literature) throughout
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Management Team (SMT); ensuring that this team reviews all medical safety data from various sources (e.g. pre-clinical, clinical trial data post-marketing, literature) throughout the development and post
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management. Key Responsibilities • Monitors the clinical safety of projects/products including activities such as literature review, evaluation of individual cases or signal detection, and responds to safety
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part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people and culture We offer plentiful benefits, state-of-the art facilities and helpful resources – all designed
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part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people (link is external) and culture We offer plentiful benefits, state-of-the art facilities and