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reproductive health, and strong interpersonal skills. This LSRP3 scientist will lead a research team focused on discovery and drug development for diseases of uterine contractility: preterm labor (too much
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and gather consent from study participants according to protocol. Assist in developing recruitment strategies. Coordinate collection of study specimens and processing. Collect and manage patient and
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consent from study participants according to protocol. Assist in developing recruitment strategies. Coordinate collection of study specimens and processing. Collect and manage patient and laboratory data
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impact on the quality of education across the world. The GSE is committed to developing leaders in education research, practice and policy. Our community includes over 60 faculty, 400 students, 230 staff
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therapeutic vulnerabilities and targets for drug development. Additionally, we are developing genomic approaches to investigate the on-target and off-target effects of different cancer drugs, with profound
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and SUP's digital publishing program. This role is responsible for essential tasks within the manuscript development process, including coordinating peer review, overseeing permissions, and preparing
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visa-related matters in partnership with Bechtel and relevant university offices. Team Supervision & Development Supervise and mentor Administrative Associates, set performance expectations, allocate
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participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing
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, and regulatory agencies. Coordinate studies from startup through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing and
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from startup through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies. Coordinate collection of study