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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. ROLE SUMMARY As a member of our NGS and Data Science team, you will
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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 A Scientist (level R3) position is available
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ROLE SUMMARY Device and Combination Product Development (DCP) is a drug/device combination product design and development organization focused on improving patients' lives through customer-focused
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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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Why Patients Need You Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure
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ROLE SUMMARY The Field Oncology Medical Outcomes Director is a field-based medical colleague responsible for providing therapeutic area/product expertise for a designated therapeutic in Oncology
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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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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 Designing new medicines at Pfizer
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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