284 information-security "https:" "https:" "https:" "https:" "https:" "UCL" "UCL" positions at University of Kansas Medical Center
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, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https
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collaboration between KUMC clinical teams, educators, and community-based partners, helping to build, strengthen, and sustain these relationships. Anticipated hiring range is $61,000 - $65,000 Job Description
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Summary: The Laboratory Coordinator is responsible for working collaboratively with multidisciplinary teams, research and hospital staff to coordinate the collection and shipment of oncology clinical trial
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with data analysis, and contribute to the overall efficiency and safety of the laboratory. This position will have hands-on experience in molecular and cellular biology research. Job Description: Job
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, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https
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of new, more efficient procedures. Collaboration: Work with multidisciplinary teams of scientists, clinicians, and regulatory experts to ensure patient safety and therapeutic efficacy; support preclinical
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that the quality assurance and monitoring plans achieve the goal of ensuring the highest quality of patient care and patient safety. Maintains knowledge of current industry standards set by professional
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, plus ten paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12
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(KUCC) Clinical Trials Office. The University of Kansas Cancer Center is the region's only National Cancer Institute-designated comprehensive cancer center where patients gain access to the most promising
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to the collection, documentation, and analysis of clinical research data. Additionally, the Clinical Research Coordinator monitors participant progress, documents and reports adverse events, and participates in