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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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well as proactively staying in the front of the current development of statistical methodologies. ROLE RESPONSIBILITIES Provide scientifically rigorous statistical input into project development plans, regulatory
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at country or regional level Responsible for PTA and SIV report review for reports completed by the Site Care Partner Supports implementation of Pfizer's Site Technology Experience systems (e.g. Shared
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, significant paid-time off, 12 paid holidays and more. Explore our robust benefit package here: https://hr.vcu.edu/current-employees/benefits/ In a world of the common, we are the UNCOMMON and UNSTOPPABLE. It's
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of outputs and compliance is maintained. Ensure appropriate tracking of labeling projects via defined procedures and optimal use of systems. Support the use and development of current and new tools
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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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and approval deadlines are met. Update related labeling documents e.g., for products within a similar class, of different dosage forms, and for generics. Support the use and development of current and
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and development of current and new tools, technologies and processes to support efficient global label development and worldwide submissions and approvals. Job Responsibilities GLLs have overall
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these cases, a fully-executed agreement with Henkel must be in place and current. All employees applying for an internal position must have a discussion with his/her manager about their interest in a job
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at country or regional level Responsible for PTA and SIV report review for reports completed by the Site Care Partner Supports implementation of Pfizer's Site Technology Experience systems (e.g. Shared