106 evolution "https:" "https:" "https:" "https:" "https:" "https:" positions at University of Kansas Medical Center in United States
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health trainees. Assist with the development of an infectious disease residency curriculum. Participate in scholarly activities to the extent that ACGME criteria for “core faculty” are met; these include
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development as demonstrated by application materials. Five (5) years of experience in conducting systematic reviews and evidence synthesis work. Experience preparing manuscripts for peer-reviewed publication
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, overseeing complex activities related to the collection, documentation, and analysis of clinical research data. This role participates in periodic quality assurance audits, supports the development of study
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curriculum development, implementation, and evaluation activities. Participate in service-related activities (serving on committees/task forces, mentoring students, etc.) to support the mission of the school
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team members. Provide support to team members and assist with Board of Directors interactions as appropriate. Participate in monthly member assessments and staff meetings. Assist with development and
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, budgeting, supervision, and policy development. This federally funded initiative supports family-school-community partnerships by strengthening school-based services, addressing social determinants of health
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academia, participate in the University’s Individual Development Plan policy for postdoctoral scholars, have a PhD or equivalent terminal degree (such as MD, DVM, PsyD, PharmD, etc.), and candidates should
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post-award processes, ensuring compliance with sponsor and university requirements. Responsibilities include coordinating proposal development and submission, overseeing award setup, monitoring budgets
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calls, and professional development sessions. Provide education and training to new research personnel and clinical staff as needed. This job description is not designed to cover or contain a
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workflows of clinic, Epic/Beacon, and any other systems required for scheduling, screening and treating new clinical trial patients. Assist leadership in the development of Standard Operating Procedures and