171 programming-"Multiple"-"U"-"U.S"-"O.P"-"St"-"Humboldt-Stiftung-Foundation" positions at University of Alabama at Birmingham
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. Employs strategies to maintain recruitment and retention rates. Prepares and submits multiple levels of research documentation (i.e., IRB, IND, or FDA submission, educational materials, reports, grant
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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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completion of certification. · OT Pay: 0~10 Hours OT/Week is expected. May exceed 10 Hours/Week under extraordinary conditions. · Benefits include Multiple Health Care Plan options, Dental
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of the immune system during health and disease and interactions between human-specific pathogens and their host. Our work is funded by multiple NIH grant awards, private foundation investments, and federal
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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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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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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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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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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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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