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processes and maintain compliance with applicable policies. Provide project management oversight of designated vendors on system design projects and other enhancement projects or initiatives. Develop
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ability and flexibility to work alternative or additional hours internally and externally (weekends/evenings/nights) to provide study activity coverage. They provide direct, face-to-face instruction and
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ability and flexibility to work alternative or additional hours internally and externally (weekends/evenings/nights) to provide study activity coverage. They provide direct, face-to-face instruction and
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for the performance of an essential function of this role including: education/licenses/certifications, location, relevant experience, technical and/or other job-related skills. Basic qualifications determine minimum
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Independently design, execute and document key experiments to enable clear go/no-go decisions; present findings to large and small audiences Provide leadership within technical area of expertise; may train others
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(FDA, EMA) and process is an asset. Evidence of continuing education/training relative to drug development/study conduct/pharmaceutical medicine is a plus. NON-STANDARD WORK SCHEDULE, TRAVEL
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characterize and develop drug candidates from early phases of development to commercial launch. As a Director in the group you will lead a team of analytical scientists to assess the chemical and physical
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software or software used in pharmaceutical or production environment. Good Laboratory Practices (part of GxP)/Good Manufacturing Practices (also cGMP) knowledge Desire to develop their own technical skill
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. Demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues