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public pharmaceutical data sources to develop and inform financial modeling decisions Partner with key internal stakeholders to develop financial analysis supporting optimal financial investment in payer
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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., QRD, PLR
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compound(s) to develop global publication and medical content dissemination plans Develop and maintain relationships with external authors through engagement with ongoing publication activities, including
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responsibilities, this role 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
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compound(s) to develop global publication and medical content dissemination plans Develop and maintain relationships with external authors through engagement with ongoing publication activities, including
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the external clinical community. Principal Responsibilities: Lead, develop and execute the strategic development of therapies for multiple medicines in prostate cancer Work across the organization and on
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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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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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-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