563 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "Helmholtz Zentrum Hereon" positions at University of Pittsburgh
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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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to, recruiting and enrolling patients into studies, imaging techniques, and analyzing and interpreting data. You will be responsible for providing regular updates to collaborators/senior scientists. You will be
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departments and acts as liaison and ensures confidentiality of high-level, sensitive information. Manages office workflow. Assists with strategic planning processes and administrative goals and priorities
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academic and career goals, select appropriate courses, and plan for degree attainment. Manages small to medium-sized, moderately complex projects. Essential Functions Must be able to use a computer and
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) techniques for the study of ESLD, accompanied by the relevant histological, biochemical, and immunological methods for analysis. The applicant will participate in data analysis, research seminars, and
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status. • Collects pertinent information and updates data bases for registry assessments and clinical trial forms. • Escorts subjects/participants to research scanning sites. • Maintains and organizes
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, configuration, monitoring, and lifecycle management. • Assists with the deployment and operation of AI enabled tools, automation platforms, and data driven services that support departmental and enterprise needs
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of particle detectors. The candidate is expected to engage in planning for deployment of these tools in view of software releases, Monte Carlo campaigns, and data taking runs of the detector. Additionally
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programming and monitoring • Fitness and clinical data collection and entry • Undergraduate research assistants supervision • Oversees research participants and equipment safety standards during exercise
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assessment and management, and recognition and escalation of adverse events, • Collect and verify study-specific physiologic and clinical data in accordance with approved protocols, SOP and GLP requirements