272 computer-security-"https:"-"https:"-"https:"-"https:"-"https:"-"https:" positions at Emory University
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contribute to the excellence of our academic community. KEY RESPONSIBILITIES: Directs the strategic planning, development, and implementation of program. Collaborates with representatives from private
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or theft. Assists in relocating materials and reconfiguring storage locations. May transport items and materials via large trucks, using proper safety and handling techniques to safeguard materials. Performs
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. MINIMUM QUALIFICATIONS: High School Diploma or GED and five years of clinical research experience. Or two years of college in a scientific, health related, or business administration program and three years
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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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to identify funding opportunities for the organization in government, philanthropy and business sectors. The position coordinates closely with Integrated Program Services teams such as External Relations
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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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Hematology Team: The Hematology Program is an integral component of the Aflac Cancer & Blood Disorders Center, with over 30 faculty members, 18 of whom are primarily clinically focused as well as 15 advance
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. MINIMUM QUALIFICATIONS: High School Diploma or GED and five years of clinical research experience. Or two years of college in a scientific, health related, or business administration program and three years
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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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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