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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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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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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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information into clear, concise, and well-structured documents that can be easily understood and followed by researchers, clinicians, and other stakeholders involved in the studies. Qualifications MD or PhD
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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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order to simulate the likely obstacles to project progression Drug Development Knowledge Technical proficiency is a key competency for this role: Technical proficiency includes experience in the use
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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
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Faculté de biologie et de médecine de Lausanne | Lausanne, Canton de Vaud | Switzerland | about 2 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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for resource requirements and providing verification execution schedules to complete project turnover. Through your comprehensive knowledge of the verification process, you will also be managing multiple
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. QUALIFICATIONS BA/BS Degree in science or health-related field MS, PhD or Pharm D preferred Has extensive knowledge of the clinical research process and Good Clinical Practices from previous employment experience