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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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development, medical scientific affairs, program management, data sciences, quality and compliance, nonclinical, medical writing and publications, and chemistry, manufacturing, and controls, as
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U.S. PhD degree candidates Additional Information Applicants should submit the following application materials by the priority deadline of October 31, 2025: 1. Curriculum vitae (CV), uploaded 2
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, including updates to Company Core Data Sheet (CCDS), US Prescribing Information, and EU SmPC. Cross-Functional Collaboration Work closely with Clinical Development, Drug Safety, CMC teams to ensure regulatory
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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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U.S. PhD degree candidates Additional Information Applicants should submit the following application materials by the priority deadline of October 31, 2025: 1. Curriculum vitae (CV), uploaded 2