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, and scholarly activities. In partnership with Northeastern University, Alnylam Pharmaceuticals is offering a two-year Safety and Risk Management fellowship, based in Cambridge, MA. About Alnylam We
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Manage, develop, and implement regulatory strategy in support of Eidos development programs. Develop proficiency within the Veeva regulatory management system where you will support the planning
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Creation of field tools and training to support external customer engagements Lead Congress planning and management (e.g., material creation, meeting tracking and sponsorship management) Evaluation and
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: · PharmD from an accredited college or university before the start of the fellowship term; · Ability to interpret and discuss complex medical scientific data; · Excellent project management, time
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to understand the drug development process and the Regulatory Affairs role – this role provides strategic and operational regulatory support to the development, commercialization and life cycle management
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availability. Medical Information Fundamentals: Content Creation Medical Information Database Management Promotional Review Product Launch Planning and Execution Development of AMCP Dossier and Payer Focused
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products. Effective support and management continue throughout Alnylam’s product life cycle. Assuming increasing responsibility over the two years, the experience gained throughout this fellowship will allow
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other clinical documents under the direction of the Medical Lead • Lead interactions with internal and external stakeholders (study sites, vendors, committees, etc.) in support of clinical trial
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in academic seminars, research, teaching, conferences, and internal presentations while developing leadership, communication, and project management skills through mentorship. Qualifications • Doctor
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, patient journey mapping, and stakeholder engagement across specialty pharmacies, distributors and wholesalers Gain exposure to trade and distribution channel management, including distribution agreements