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, in conjunction with country intelligence to proactively identify risks to quality and compliance and to develop and implement mitigation plans to address these risks. Site Care Partner Level 2 may be
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interphase with pharmacologists, PK/PD modelers, and clinical pharmacokineticists to develop a translational pharmacology plan, human pharmacokinetics and dose projections for clinical candidates. As a PDM
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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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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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trusted relationships with our partners, including patients and patient organizations. The Participant Experience & Ecosystem team leads the centralized delivery of content, channels and education to
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-on interactions with automated, liquid handling systems and an expert knowledge of our workflows and systems with the expectation to provide immediate assistance, education, and training and lab tours
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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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Medicine Therapeutic Area. Your project management skills will be leveraged to develop clinical trial timelines and oversee budgets for the assigned clinical studies/programs. Your ability to partner and
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director to develop and apply interdisciplinary approaches to understand the mechanisms of action of different types of RNA-based viral vaccine drug substance and lipid nanoparticle drug products and