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to support decision making in the drug development process. The General Toxicology R6 Study Director is responsible for the design, conduct, interpretation, and reporting of exploratory, mechanistic and GLP in
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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. What You will Achieve We are seeking a highly motivated chemical
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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. What You Will Achieve Drug Safety Research & Development (DSRD) is
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Products (MDCP) Quality Operations team within the Pfizer Global Supply (PGS) organization. The incumbent provides quality assurance leadership/guidance of MDCPs related to design controls (21 CFR 820
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data infrastructure Design, develop, optimize, and maintain data architecture and pipelines (e.g., feeding medical data sources into data lake for ongoing projects) Partner with product manager and data
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data infrastructure Design, develop, optimize, and maintain data architecture and pipelines (e.g., feeding medical data sources into data lake for ongoing projects) Partner with product manager and data
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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. What You Will Achieve As a Senior Scientist, you will be
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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. What You Will Achieve As an Associate Scientist, you will be
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to Clinical Study Protocols, Clinical Study Reports, Clinical Pharmacology plans for programs. Provides clinical pharmacology expertise to oncology project teams including planning, design, and oversight
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disease states to optimize doses, dosage regimens and study designs throughout all phases (first-in-human through post-approval) of clinical drug development. With guidance, identify opportunities where