171 programming-"Multiple"-"U"-"Prof"-"U.S"-"University-of-California"-"O.P" 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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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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for the comprehensive planning, implementation, and coordination of internship and practicum activities for multiple Master's programs. Duties & Responsibilities Coordinate Internship/Practicum Rotations: Arrange and
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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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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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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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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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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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initial and final submission to the UAB Office of Sponsored Programs (OSP). To serve as an advisor and reporting to the Director of Research Administration-Shared Services, identifies, reviews and makes
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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