88 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "UCL" research jobs at University of Michigan
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Concepts and Research Design Ethical Participant Safety Considerations Investigational Products Development and Regulation Clinical Study Operations (GCPs) Study and Site Management Data Management and
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study's data collection by helping with study participant recruitment, data and biospecimen collection, scheduling study visits and the family experience. We are looking for a candidate who can autonomously
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. What You'll Do The candidate will join a multidisciplinary team focused on accelerating drug discovery with data-rich and automated chemical methods. We are a medicinal chemistry lab with expertise in
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, data collection, and general team support. The position is term-limited based on the current funding period (ending August 2027), and continuation is subject to additional funds. Mission Statement
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meaningful information from noisy or ambiguous sensory signals? To what extent does neural plasticity in the auditory system occur via mechanisms dictated by classic theories of reinforcement learning, or does
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techniques (DNA extraction, PCR, gel electrophoresis, amplicon purification) General laboratory upkeep (racking tips, glassware cleaning, identifying supplies for reorder) Data analysis DNA sequence assembly
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research projects such as registries, retrospective data reviews, long-term follow-up, and other non-interventional studies. Our research coordinator program is well established, and considered an integral
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) plus fellow benefits. Information about available benefits can be found here . Job Summary The Project Dr. Melynda Price, Director of the Institute for Research on Women and Gender at the University
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design and performance according to standard design control and quality system practices. 3. Collate, combine, and present experimental data in a clear and concise manner. Use appropriate statistical
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clinical research studies. Seeking highly motivated, positive, organized, and autonomous individual. As a member of this team, you will collect primary data, schedule participants, assist with regulatory