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formalization of campus-wide IT prioritization processes, including mechanisms for evaluating, sequencing, and aligning initiatives with institutional strategy. Develop and sustain governance models and
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and contact information. Aligns team actions with calendars, milestones, and virtual workspaces. Assists with coordination of program events, workshops, presentations, and visitors. Provides additional
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ensuring priorities are clearly aligned, initiatives are strategically sequenced, roles and responsibilities are well understood, and teams are set up for success. About the Role Reporting to the Director of
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initiatives aimed at scaling laboratory throughput capacity. Reporting to the User Support Analysis Group Lead, this position leverages bioinformatics tools to process data from multiple sequencing platforms
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, including single-cell RNA sequencing (scRNA-seq), spatial transcriptomics, and genomic sequencing, contributing directly to the identification of key molecular drivers and therapeutic vulnerabilities in
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characterizing patient-derived microglia-integrated nigrostriatal assembloids to investigate neuroinflammation in the pathogenesis of Multiple System Atrophy (MSA) and to evaluate therapeutic modulation
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University of California, San Francisco | San Francisco, California | United States | about 2 months ago
allocations, workflow sequencing, and laboratory timelines, supporting multiple investigators and multi-project laboratories Academic knowledge and skills dependent on area of specialty (laboratory research
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or more disciplines that align with the theme for the research stream Effective communication skills Ability to manage multiple responsibilities and timelines simultaneously Ability to work both
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Registrar teams, functional leads, and academic stakeholders to interpret complex program rules, configure audit logic, validate outcomes, and ensure alignment with institutional governance and published
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involved in the domestication process. - Analysing whole genome SNP variability in a collection of Brassicas aligned to the the super-pagenome, assessing whole genome variability and identifying regions