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regulatory requirements mandated by federal, state, and accrediting agencies. Responsible for data collection, analysis and recommendations for patient focused process improvements, engaging stakeholders as
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. Responsibilities* Analysis: Perform data analysis and problem solving in a complex healthcare environment using clinical data to deliver healthcare information to transform care delivery at Michigan Medicine
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PCR and RNA sequencing, perform bioinformatic analysis of RNA sequencing data Non-experimental job responsibilities will include: Lab Maintenance: Share responsibilities in maintaining laboratory
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team to develop, design, and assist with M-FLIP projects and initiatives. Potential projects may include assisting with an ongoing analysis of extreme risk protection order (ERPO) usage in the state
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: Quantitative Social Science Analysis and Big Data. A 35% appointment requires teaching 2 laboratory sections per week, and a 70% appointment requires teaching 4 laboratory sections per week, each under
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adherence to data management protocols throughout the full data lifecycle from collection to analysis Regulatory & Administrative Excellence: Manage IRB applications, facilitate university contracts, and
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experimentation, metabolomics and transcriptomics studies, and organization and curation of tissue samples; conduct statistical analysis of data and interpret/discuss research with the principal investigator, lab
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, medical conditions including those related to pregnancy, childbirth and breastfeeding, arrest record, or any other factor where the item in question will not interfere with job performance and where
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critical component of this job's responsibilities. Demonstrated multi-tasking skills and ability to prioritize workload efficiently are essential. The CRC will work collaboratively with other team members
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Medicine and Bioinformatics. The specific objectives of the project are to (i) deploy network analysis methods to genomic data (50%), and (ii) develop such algorithms including community detection algorithms