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. Plans relevant PK/PD analyses. Is responsible for integrating knowledge of pharmacokinetics, pharmacodynamics, patient characteristics, and disease states to optimize doses and dosage regimens throughout
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. Through your comprehensive knowledge of principles, concepts and theories of the discipline, you will also work towards advancing new concepts and methodologies. You will be able to take a cross functional
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conveying messages in a clear and concise manner. Analyzes, interprets , and distills data and other information to create documents . Applies comprehensive knowledge of relevant regulatory requirements and
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allocation and risk management. As Associate Director, your advanced knowledge of the principles and concepts of project management and comprehensive knowledge of other vaccine research and development
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for use of innovative analytical methods to integrate knowledge of pharmacokinetics, pharmacodynamics, patient characteristics and disease states to optimize doses, dosage regimens and study designs
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, cross-function and external continuous improvement efforts. Maintain up-to-date knowledge of biomarker assay technologies and clinical laboratory standards, regulatory guidance (e.g., GLP, GCLP), and
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rates and ensuring zero down time. As a Manager Automation Engineer working with the Strategic Automation team, your knowledge and skill will be utilized to support a variety of customers. Our team
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Faculté de biologie et de médecine de Lausanne | Lausanne, Canton de Vaud | Switzerland | 3 months ago
medicine. Desired profile: PhD in molecular biology and/or biochemistry. Ability to work interdisciplinarily. Demonstrated ability to supervise and manage a group of at least 10 to 15 scientists in both
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what it takes to bring large molecules to commercialization. The successful applicant will be a strategic leader and will prioritize development of scientific staff. They will apply their knowledge and
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. Advanced academic qualifications/degree such as PhD an advantage but not essential. Experience and Attributes: At least 8 years of pharmaceutical labeling experience associated with content development and