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to develop and manage plans will achieve objectives, interpret internal and external business challenges and recommend best practices for improvements. It is your commitment and hard work that will make Pfizer
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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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the organization to drive the implementation of improvement initiatives in response to potential and real risks of AI to pharmacovigilance quality and compliance within the company. ROLE RESPONSIBILITIES Develop and
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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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to develop forward thinking programs that maximize medical and commercial value. Applies extensive expertise and in-depth knowledge of the vaccine development process and project management tools to drive team
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of study/submission level statistical deliverables on assigned projects. Ensure that all statistics activities are conducted in compliance with relevant regulatory requirements and Pfizer standards. Develop
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bio-functional assays, including information/data archiving, Standard Operating Procedure and status reports. Assist in ordering supplies from internal inventory and prepare reagents/supplies necessary
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diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful
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within Pfizer Oncology R&D, including content and structure of leadership updates. Develop and present quality point of view at Pfizer Oncology R&D governance meetings. Advise asset/study team