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data science driven support for an assigned brand and will partner with US Commercial, business, and digital teams, to develop and implement models, insights, and data products that drive brands
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documents such as Pre-INDs, INDs, BLAs, and IMPDs. Collaborate with regulatory partners to prepare Orphan Drug Designation (ODD) requests based on pre-clinical efficacy data and disease prevalence, submitting
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Achieve It Design, develop, deploy and test our automated processes, systems and equipment. Contribute substantially to the interpretation of results and the design of subsequent activities. Maintain and
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equipment. The Manager will report to the Faculty Director and carry out the following functions: Maintenance, ordering, and day-to-day upkeep of the cryo-EM Facility. Prepare samples, operate microscope, and
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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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disciplines will enable you to lead complex projects across the division. Your ability to develop and manage plans will facilitate achieving objectives, interpreting internal and external business challengesand
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compliance. Provide subject matter expertise and guidance to colleagues. Lead / co-lead complex pilot studies and projects across preclinical Pfizer Oncology enterprise. BASIC QUALIFICATIONS PhD with 4+ years
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boards, as well as advisor identification and engagement. Provide high-quality scientific/clinical input and review of educational grant requests, and publications as needed. Provide scientifically
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that will make Pfizer ready to achieve new milestones and help patients across the globe. How You Will Achieve It Contribute to the completion of projects, manage own time on agreed targets, develop plans
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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