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. * Oversee layout, allocation, and tracking of space among multiple labs; manage logistics of laboratory moves; implement plans for renovations of equipment and or/facilities in collaboration with facilities
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; determine proper method of repair. · Oversee layout, allocation, and tracking of space among multiple labs; manage logistics of laboratory moves; implement plans for renovations of equipment and or
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and OR environment. Regular collaboration with medical teams, including nurses and pharmacy staff, will be essential. The CRC2 will develop and maintain specialized databases, such as those tracking
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those tracking enrollment, ICU outcome metrics (e.g., ventilator days, organ failure scores), and lab specimen data. They will regularly evaluate data collection processes, identifying areas
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, identifying standard of care versus study procedures. Track patient and study specific milestones, and invoice sponsors according to study contract. Ensure regulatory compliance. Regularly inspect study
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best practices. Develop study budget with staff and principal investigator, identifying standard of care versus study procedures. Track patient and study specific milestones, and invoice sponsors
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a trial; track physician compliance. Assist with analysis of data and preparation of manuscripts and scientific presentations. * - Other duties may also be assigned. DESIRED QUALIFICATIONS: Clinical
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process, using data-driven metrics to track efficiency, identify bottlenecks, and deploy resources strategically to maintain optimal timelines and outcomes. Establish and advance a cohesive, enterprise
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, identifying standard of care versus study procedures. Track patient and study specific milestones, and invoice sponsors according to study contract. Ensure regulatory compliance. Regularly inspect study
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, ensuring accurate and timely tracking of costs and payments across the project delivery portfolio. * - Other duties may also be assigned MINIMUM REQUIREMENTS: Education & Experience: · Bachelor's