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expert 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
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cross-functional team(s) throughout the product life cycle. Key responsibilities: Acts as the SME for relevant TA(s) •Has an in-depth knowledge and understanding of the unmet medical need, SoC (standard
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for the integration, analysis, and evaluation of internal and external safety information through product lifecycle management, and evaluation of internal and external safety information through product lifecycle
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The location of the position will be at our Cambridge, MA site and will not have the ability to be located remotely. Hundreds of millions of people globally are negatively impacted by
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This position is written for Director - we can hire Associate Director for those with careers that include less established science / clinical study experience. We support International family
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, or in order to perform the essential functions of a position, please send an e-mail to [email protected] call +1(877)395-2339 and let us know the nature of your request and your contact