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Assistant will manage multiple senior leadership calendars and travel arrangements, administratively support RA-wide meetings and projects, and serve as a collaborative team member within the RA
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of Kansas Medical Center will be responsible for independently managing and coordinating multiple, complex Phase I–IV industry-sponsored, investigator-initiated, and federally funded clinical trials
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Description Summary: Provides project management, risk management, and day-to-day coordination of multiple complex clinical trial projects from protocol development to study close-out for the Environmental
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: The Regulatory Coordinator is responsible for performing study-specific regulatory and safety reporting across multiple studies. This will be accomplished by: assuring the research is compliant with applicable
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nationally and internationally for our innovative work in stroke recovery including our work on high intensity interval training to improve walking outcomes post-stroke. We have multiple research
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, multi-channel radio system. Operates multiple computer workstations for the purpose of documenting calls for service, sending and receiving inter- and intra-state information related to wanted persons
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treatments. As part of a centralized research team supporting multiple departments and medical specialties, the Sr. CRC collaborates with multidisciplinary teams to coordinate all aspects of clinical research
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Insights. Experience working in cross-functional business teams and handle multiple concurrent tasks. Experience working in a higher education shared service center environment Experience working with Budget
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. Experience in administration, project development, and financial management. Experience managing multiple complex assignments. Preferred Qualifications Education: Master's degree. experience may substitute
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organizational skills Strong problem-solving skills Manage multiple tasks and timelines Required Documents Cover Letter/Resume Comprehensive Benefits Package: Coverage begins on day one for health, dental, and