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Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic
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a broad understanding of the biotechnology industry landscape, including drug development processes and organizational dynamics. Program Overview: Year 1: Foundational Training and Cross-Functional
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an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve
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, processes, regulations, and compliance that aligns with industry standards. Create, update, and facilitate review of medical response documents for call center communications to healthcare providers and
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, create, test and deliver transformative medicines to treat patients who suffer from genetic diseases. BridgeBio's pipeline of development programs ranges from early science to advanced clinical trials
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, processes, regulations, and compliance that aligns with industry standards. Create, update, and facilitate review of medical response documents for call center communications to healthcare providers and
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and participate in the development of Regulatory Department systems and processes Assist with performance and compliance metrics for internal and external responsibilities Collaborate with internal
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prompt and accurate, quality-assured documents are created in alignment with the Global and Regional Medial Affairs scientific messages and strategy. Creates and implements processes/procedures for a
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, including labeling, regulatory strategy, and chemistry, manufacturing, and controls (CMC). Labeling Management: Aid in strategic guidance on product labeling throughout the product life cycle. Process
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clinical data regarding marketed and investigational products and/or therapeutic areas of interest to Abbott. Support the overall operations of a medical information function by participating in process