657 algorithm-development-"Multiple"-"Simons-Foundation"-"Prof" "UNIS" positions at University of Minnesota
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completeness Maintain up-to-date, confidential patient records in compliance with HIPAA Prepare materials for new patient visits and coordinate documentation needs Payment & Insurance Processing - 10% Collect co
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the complex interactions between ecosystem function and environmental change at multiple scales, ranging from micro to macro and local to global. Developing appropriate climate change mitigation and adaptation
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intern in multiagent trajectory optimization. The successful candidate will help develop and implement mixed-integer and nonlinear programming methods for coordinating multiagent UAV systems. This role
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intake, student check-out with a positive and friendly demeanor Must be a team player, working collaboratively with co-workers and faculty Demonstrated ability to function with multiple priorities and
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projects focused on patient-provider communication and health equity. This role is ideal for someone with research experience who thrives in a collaborative environment, is comfortable managing multiple
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(PI and Co-I) and the cytokine reference laboratory in developing assays, scheduling the assays and receipt of data. 10% effort: Writing grants, study protocols, reports, publications and presenting
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of Pharmacy. This includes the development and progression of professional pharmacy students, along with the design, development, maintenance, and implementation of the professional Pharm.D. curriculum
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of lab activities. The CNS lab is a multiple PI-led research lab with a significant grant funding portfolio across multiple departments (Pediatrics, ICD) housed at the Masonic Institute for the Developing
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to academic operations and faculty development. Key Responsibilities: • Initiate and oversee the yearly performance review process for all faculty within the department • Serve as the primary liaison with
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submissions to ensure deadlines are met. In collaboration with the PI, interpret study protocols and develop consent form documents needed for each clinical research study in conjunction with central CTSI