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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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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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PHYSICAL/MENTAL REQUIREMENTS Sitting, ability to perform complex data analyses Work Location Assignment:On Premise The annual base salary for this position ranges from $99,900.00 to $166,500.00. In addition
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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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of data and analytical solutions Lead the evaluation, implementation and deployment of emerging tools and analytic data engineering process in order to improve team productivity BASIC QUALIFICATIONS
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of data and analytical solutions Lead the evaluation, implementation and deployment of emerging tools and analytic data engineering process in order to improve team productivity BASIC QUALIFICATIONS