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that the current version of consent forms are completed, and that the informed consent process is properly documented and filed. Review medical history to determine eligibility status. Schedules, coordinates
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mail Coordinate catering when needed Schedule meetings for internal and external participants Manage conference room reservations assigned to the Division Process facilities requests Ensure DRS suite is
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. Specific duties include: Design and Performance of Research Experiments (75% of Time Spent) Mechanism based discovery of cancer therapeutics. Characterization of metabolic processes of leukemia stem cells
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vision for computer work; CU is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws governing nondiscrimination in employment. We are committed to creating a
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with a general science background to support Quality Assurance and radiation measurement tasks within the Department. This position requires excellent computer skills, technical problem solving skills
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history and current medication information, reviews research protocol Inclusion/Exclusion Criteria, and confirms eligibility of subject to participate in clinical trial. Performs informed consent process or
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processes and procedures. Excellent time management and organizational skills with the ability to work independently, prioritize tasks, work under tight deadlines. Flexibility and the ability to adapt
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throughout the employment application process. To request an accommodation pursuant to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator at hr.adacoordinator@ucdenver.edu
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to applicants with disabilities throughout the employment application process. To request an accommodation pursuant to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator
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in TRUE, and as they begin the transition to adult care process, maintain high ethical standards and compliance with healthcare regulations in all aspects of patient transition coordination, ensuring