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collaboration with internal cross-functional teams and engagement with external experts on key company initiatives. The Fellow will be immersed in publication and medical communication activities related
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Requirements for Pharmaceuticals for Human Use (ICH), Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and other relevant global guidelines to ensure compliance of regulatory strategies and
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. Responsibilities • Develops and maintains a broad knowledge of medical, scientific, and technical information for therapeutic area and product portfolio, becoming a scientific influenza expert for Medical
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, legal, and clinical development) to communicate up-to-date data generation plans and needs as a subject matter expert Support the RWE/HEOR team in overseeing operational activities for the team's projects
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, congress planning, and vendor coordination, including ensuring alignment with internal policies, Good Publication Practice guidelines, compliance requirements, and authorship criteria • Supporting consistent
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the Medical strategy and leads Medical execution to support the development of Alnylam’s investigational RNAi therapeutics. Early Assets Medical Affairs partners with experts across the organization to guide
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to inform decision-making, thereby becoming a subject matter expert in the assigned therapeutic area(s) Assist in the planning and execution of medical congresses, advisory boards, healthcare provider
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force for good, and an environment for innovation in the life sciences and other high-growth sectors. Together, we envision an innovation corridor that in the coming years will stretch from Boston