566 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "Newcastle University" positions at University of Pittsburgh in United States
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Center (which serves undeclared students) on the major declaration process and transition to major advising; advisor training and mentoring; assessment of advising; and the use of data/research to monitor
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clinical staff in the planning and implementation of patient care. Observes, documents, and communicates to the physician and/or other clinical staff symptoms, potential problems, and pertinent information
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not limited to screening, recruitment, scheduling, conducting study visits, collecting data and data entry. The candidate will be supported by dedicated regulatory staff to assure IRB and fiscal
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or administrative departments. Essential Functions Requires the ability to visualize a computer screen, to work with computer hardware and software, to communicate verbally and in writing, and to use a phone. The
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an experienced technician capable of independent experimental execution, advanced wet-lab and omics workflows, and intellectual contribution to experimental design and data interpretation. The Research Technician
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. Three representative writing samples. 5. Names and contact information for least six professional references (please note: written copies of letters of reference will be required for all
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recruitment, monitoring study implementation, and data management. It is also critical that the coordinator ensure compliance with University and VA Pittsburgh Healthcare Systems Institutional Review Boards
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for participation or continued participation after enrollment with exception from informed consent, and reliably ascertains primary study outcomes. Completes accurate data collection, audits research studies
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campus locations. Must be able to lift and transport computer equipment weighing up to 30 pounds to various campus locations. The University of Pittsburgh is an equal opportunity employer / disability
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-Marie Lavenburg. Candidate will recruit research participants for clinical trial including conducting the informed consent process (over the phone). Complete data collection for study visits and enter