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in a specific therapeutic area to lead a longitudinal project across Medical Affairs. · Develop a working knowledge of various departments, processes, regulations, and compliance that aligns with
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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
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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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, 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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benefits package for benefit eligible employees. This includes medical, vision, dental, paid time off, tuition assistance, wellness & life, retirement- as well as commuting & transportation. Visit https
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, Switzerland, and UK - among others. At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that
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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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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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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