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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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, 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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. 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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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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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 that will
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throughout the labeling review and approval process through notification to stakeholders in order to ensure that these documents are produced in a timely manner according to internal SOPs and external
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Manager, Study Start Up Project Manager, Site Intelligence Lead, Country Trial Manager, Site Excellence Partners, Site Relationship Partners, Site Care Partners, Contracts Lead, Regulatory Affairs, pCRO and
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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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team targets and lead tasks and initiatives will help in completing critical projects. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and
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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