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Clinical Research and may take the lead on company-wide, global process improvement initiatives, and champion's process enhancements and solutions for complex issues. Leads change for Vaccine Clinical
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sub team(s) to ensure collaboration and seamless connectivity. ROLE RESPONSIBILITIES Responsibility to assist/lead development and execution of simple to moderately complex clinical studies; on more
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. This role is accountable for study start up, activation, and execution to the plan for targeted sites. In addition to the main point of contact, the lead will help coordinate with other roles and functions
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development process. Collaborates with project teams, subject matter experts, and quality lines to e nsure clear, factual, effective, and appropriately concise presentation of analyses and associated
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their own time to meet objectives; forecasts and plans resource requirements (people, financial, and technology) for projects within VRD. Provides guidance to and/or may lead/co-lead moderately complex
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, prioritize multiple demands, and effectively lead in a matrix organization. PHYSICAL/MENTAL REQUIREMENTS NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Travel: approximately ~20% Attendance
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affairs and comprehensive knowledge of other disciplines will enable you to lead complex projects across the division. While managing complex project environments, you will be able to anticipate and
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will coordinate with other roles and functions that will interface with study sites (eg. Study Monitor, Investigator Contracts Lead, Site Activation Partner, Clinician, etc.) thereby, optimizing
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. Job Summary The Global Labeling Lead (GLL) has overall accountability for the initial creation and relevant updates to labeling documents for their assigned products. This includes guiding the Labeling
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revising the label. The LOM provides project management to the Labeling Team throughout the labeling review and approval process through notification to stakeholders in order to ensure that these documents