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, e.g., GDMS. Finalize documents post QC (including update of GDMS document properties such as entry of PfLEET2 number, update of document title, update CDS cover page etc.). Manage the document status in
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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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Manager may be responsible to independently take on the closing out of one or more studies post database lock. Provides back up to or takes on the responsibilities of Global Study Manager as needed
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Maintain, update, and support Pre & Post deal analytics, Formulary tracking, Market Dynamics, and Op Planning BASIC QUALIFICATIONS Candidate demonstrates a breadth of diverse leadership experiences and
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repository Finalize documents post QC Manage the document status in document management system and notify internal stakeholders of the availability of labeling documents. Create and QC SPL (xml) for USPIs
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, e.g., GDMS. Finalize documents post QC (including update of GDMS document properties such as entry of PfLEET2 number, update of document title, update CDS cover page etc.). Manage the document status in
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Pfizer processes and systems. The GLL also interfaces with Hub Labeling Managers and Pfizer Country Office (PCO) colleagues to support timely and quality submissions globally. The GLL will support the use
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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
-
Manager may be responsible to independently take on the closing out of one or more studies post database lock. Provides back up to or takes on the responsibilities of Global Study Manager as needed
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, and support Pre & Post deal analytics, Formulary tracking, Market Dynamics, and Op Planning BASIC QUALIFICATIONS Candidate demonstrates a breadth of diverse leadership experiences and capabilities