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potential impact to other areas of the business. Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and
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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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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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processes and maintain compliance with applicable policies. Provide project management oversight of designated vendors on system design projects and other enhancement projects or initiatives. Develop
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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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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
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in accordance with agreed upon timelines. Contribute to the training of colleagues on quality standards and processes. Develop and sustain constructive relationships within other Pfizer lines including
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statistical deliverables on assigned projects, including timeliness and quality of deliverables according to project plans. Develop effective collaborations with others within clinical teams, partner lines
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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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/ ongoing work activities of moderate complexity within the Operating Unit . Develop overall strategies for maintenance programs to include production equipment, production support equipment, utilities