302 computer-security "https:" "https:" "https:" "https:" "UCL" positions at Emory University
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of college in a scientific, health related, or business administration program and seven years clinical research experience Or licensed as a Practical Nurse (LPN) and six years clinical research experience
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, supervises and evaluates staff. Performs related responsibilities as required. MINIMUM QUALIFICATIONS: A bachelor's degree in computer science, management information systems, engineering or a related field
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scaffolding, and lift 50 pounds. Proficiency with various personal computer software applications. Must be able to wear and use appropriate personal protective equipment. Must satisfactorily pass a Medical
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scientific, health related or business administration program and five years of clinical research experience Or licensed as a Practical Nurse (LPN) and four years of clinical research experience Or bachelor's
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on program health, ROI, and strategic pivots Establish rigorous program management discipline: milestones, dependencies, risk mitigation, resource allocation, and stakeholder communications Build business
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Competencies: Data Analytics and Assessment, Public Health Sciences, Communication, Health Equity, Community Partnership, Policy Development and Program Planning, Leadership and Systems Thinking. ADDITIONAL JOB
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Competencies: Data Analytics and Assessment, Public Health Sciences, Communication, Health Equity, Community Partnership, Policy Development and Program Planning, Leadership and Systems Thinking. ADDITIONAL JOB
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Competencies: Data Analytics and Assessment, Public Health Sciences, Communication, Health Equity, Community Partnership, Policy Development and Program Planning, Leadership and Systems Thinking. ADDITIONAL JOB
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collaboration with sites, the Senior Epidemiologist, and the Informatics Business Unit Director Provides clinical expertise and guidance to sites on the DeCoDe process and results Provides clinical and analytic
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institutional guidelines. The Clinical Trials Monitor will conduct comprehensive monitoring activities throughout all phases of clinical trials, safeguarding data accuracy, participant safety, and compliance with