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documents. Global Labeling Gain in-depth knowledge of labeling regulations regarding Company Core Data Sheet (CCDS), US Package Insert (USPI), Summary of Product Characteristics (SmPC), and Structured Product
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the collection, interpretation, and presentation of safety data in internal forums Support signal detection and management activities with lead safety physicians and PV scientists Engage in safety data review
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orthosteric) and ion channels (a4b2 nAChR, a7nAChR, a9* nAChR, GIRK1/2, GIRK1/4etc.). Key initial responsibilities will include biochemical and ADME/PK studies and data analysis, SAR hypothesis generation
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scientific and strategic assistance to safety product leads to support Alnylam products · Participate in the collection, interpretation, and presentation of safety data in internal forums · Support
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internal partners and delivers on the medical plan. US Medical directors play a key role in informing global product development and data generation strategies with perspective of US Region. The team also
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documents. Global Labeling Gain in-depth knowledge of labeling regulations regarding Company Core Data Sheet (CCDS), US Package Insert (USPI), Summary of Product Characteristics (SmPC), and Structured Product
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external engagement strategy and execution, including for congresses and advisory boards Contribute to the development and planning of scientific platforms, communications and training materials, data
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internal partners and delivers on the medical plan. US Medical directors play a key role in informing global product development and data generation strategies with perspective of US Region. The team also
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practical clinical knowledge to enable efficient and effective drug development. Clinical Scientists contribute throughout the development cycle from Phase 1 to IND submission. They are data-driven
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. Throughout the fellowship, the fellow will engage in projects to learn and understand different disease states, product data, and the roles and functions within Medical Affairs. The fellow will develop