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, external alliances or committees, consortia and academic relationships. BASIC QUALIFICATIONS PhD in Pharmacometrics, Clinical Pharmacology, Pharmacokinetics, Engineering, Pharmaceutical Sciences, or PharmD
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Current knowledge of Oncology research, drug discovery and development PHYSICAL/MENTAL REQUIREMENTS Lifting, sitting, standing, walking, bending, ability to perform mathematical calculations and ability
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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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. Previous Field Medical experience PharmD, PhD, or equivalent t erminal d octo ral degree ( e.g., Doctor of Nursing Practice , Doctor of Physical Therapy ) preferred PHYSICAL/MENTAL REQUIREMENTS: Sit for
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. Previous Field Medical experience PharmD, PhD, or equivalent t erminal d octo ral degree ( e.g., Doctor of Nursing Practice , Doctor of Physical Therapy ) preferred PHYSICAL/MENTAL REQUIREMENTS: Sit for
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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
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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 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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resources to ensure all functional device activities are completed on schedule following the Pfizer Design Control process. Utilize technical writing and statistical data analysis skills to write protocols
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with 8 years of experience OR a bachelors with at least 5 years of experience OR Masters Degree with more than 3 years of experience, OR a PhD with 0+ years of experience. 5+ years of demonstrated