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able to operate independently on project teams, although, may need instruction on more complex or unusual study challenges and/or tasks. Serve as technical support for clinical issues raised by internal
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Will Achieve You will help Pfizer develop and implement chemistry, manufacturing and controls (CMC) regulatory strategies for small and/or large molecules to meet global regulatory requirements
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escalating to appropriate teams to respond and resolve questions. Follow up and close issue status with investigators to ensure awareness of resolution. Inform and educate investigator sites of Pfizer pipeline
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will utilize and interpret data from analytic tools, in conjunction with country and regional intelligence to proactively identify risks to quality and compliance and to develop and implement mitigation
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data sources to develop and inform financial modeling decisions Partner with key internal stakeholders to develop financial analysis supporting optimal financial investment in payer access. Utilize
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, sealants and functional coatings. With our trusted brands, our cutting-edge technologies and our disruptive solutions, you will have countless opportunities to explore new paths and develop your skills. Grow
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Labeling reviewers and Regulatory Authorities. Prepare comparison tables for labeling team discussions. Edit and format labeling documents- Ensure the document complies with the appropriate template (e.g
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nonclinical safety studies. Provide critical experimental design input for in vivo and in vitro studies. Develop automated statistical solutions to increase the efficiency of DSRD study conduct and reporting
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to continue this tradition by leading and growing an education and training program that will develop the next generation of leaders. This program involves a mixture of asynchronous and synchronous learning
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Team to develop and maintain Core Data Sheets (CDS), United States Package Inserts (USPI), Summary of Product Characteristics (SPC) for products registered in the EU via the Centralized, Mutual