169 programming-"Multiple"-"U"-"U.S"-"O.P"-"Washington-University-in-St" positions at University of Alabama at Birmingham
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. This position will support the DOM Clinical Research Enterprise and its shared services. General Responsibilities To prepare, submit, and assist with multiple levels of research documentation (i.e. IRB
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multiple sponsors, consortia and complex business arrangements. Drafts, reviews and negotiates industry outgoing subcontracts/amendments for research projects that require contractual negotiation and
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Programs in negotiating contracts and amendments related to the conduct of clinical research activities. Assists in preparing, developing, reviewing, and negotiating industry and sponsored research clinical
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unhoused population to include inventory, operational and financial support of the program. Responsible for administratively managing a large or complex University program or multiple programs. Provides
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office type environment preferred, but not required. Ability to lead a team of administrative professional and handle multiple tasks in a fast pace environment. Must have strong organizational and time
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supervise clerical staff. Knowledge, Skills, Abilities & Work Characteristics Advanced proficiency in PC applications, software, and database management Ability to manage multiple tasks efficiently and
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Clinical and Translational Research Program focused on cardiovascular genetics, multi-omics, and computational medicine. The successful candidate will contribute to research projects involving polygenic risk
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University or departmental policies and procedures May oversee fiscal management of grants and other funds May manage multiple programs simultaneously Exercises independent judgment to determine the best
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· Working in confined spaces · Working within extreme temperature ranges Work Schedule and On-Call Requirements: Multiple shifts available. Incumbent must have flexibility due to on-call requirements
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aspects of research program and clinical studies including education/teaching. To oversee and manage multiple clinical research protocols and the associated personnel. To design best practices