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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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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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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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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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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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, 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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are committed to diversity as well as diverse faculty who will be role models for our students. Eligibility: An MD, DO, PhD, or MD/PhD (or equivalent). Be eligible for appointment as an associate or full
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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
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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