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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 Drug Safety Research & Development (DSRD) is
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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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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
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salary for this position ranges from $74,900.00 to $124,800.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 7.5% of the base salary
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for the newly designed audience process and analytics strategies, creating best practices and data led decisioning. This is a unique role, that will curate audience data insights for enterprise-based media
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of new risks and evolving existing risks in relevant Quality Risk Management (QRM) tools. Provide feedback to QRM Business Process Owner (BPO) to continuously improve Integrated Quality Management Plan