325 embedded-system-"https:"-"https:"-"https:"-"https:"-"UCL"-"UCL"-"UCL" positions at Tulane University
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to research grant and/or contract activity • Knowledge of University policies and procedures relating to grant and contracts activity • Knowledge of University processes, systems and offices related to and/or
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participation, and occupational sectors, with a focus on Louisiana and the Gulf South. This position is responsible for building and maintaining clean, well-documented datasets; producing descriptive analyses
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, LA Summary The Assistant Director is responsible for the Center wide assessment and research portfolio, promoting and supporting community-engaged research across CPS’ constituencies and advancing
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This position is classified as "exempt, salaried" and is assigned to pay grade 27. Tulane offers a variety of options to enhance your health and well-being so that you may enjoy more out of life now and in
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including the reconciliation process Knowledge of University processes, systems and offices related to and/or involved in grant and contract submission and management Ability to work independently with
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• High School Diploma/equivalent Preferred Qualifications • Bachelor’s Degree in a biological related field is strongly preferred • Experience working with patients in a clinical or hospital setting is
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, and improves the Research Compliance Program, a university-wide compliance effort to prevent violations of law and applicable university policies and procedures. This is a high-profile, high-volume
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Summary The Senior Administrative Program Coordinator, Office of Gift Planning, provides professional support for the Office of Gift Planning. This position is also responsible for tracking and identifying
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with institutional priorities. Responsibilities include planning, execution, and monitoring of projects, system implementations, and process improvement initiatives. The Project Manager serves as a
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required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As the primary resource for protocols, the Clinical Research Coordinator acts