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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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requires understanding of GCP and GMP to support the regulatory requirements and needs of different study types, quality management, inspection readiness, audit/inspection process, clinical trial processes
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required to perform analytics Oversee data systems holding in close collaboration with data mgmt. lead and ensure accurate collection, storage, and processing of data within team Enhance data infrastructure
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required to perform analytics Oversee data systems holding in close collaboration with data mgmt. lead and ensure accurate collection, storage, and processing of data within team Enhance data infrastructure
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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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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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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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, pharmacometrics tools, software, hardware, and/or related business processes ROLE RESPONSIBILITIES With guidance, provide MIDD expertise on multidisciplinary development teams, working closely with clinical