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During the one-year fellowship, the F.A.S.T. fellow will learn about clinical trial design, including novel clinical trials for rare genetic pediatric NDDs including N-of-1 trials, development of specialized programs for clinical management of these conditions with accommodation of experimental treatments, and new outcome measure and biomarker development for these populations.
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Alteryx, Banking, Business, Critical Thinking, Data Acquisition, Data Analysis, Data Management, Data Operations, Data Quality, Decision Making, Financial Products, Leadership, Management Reporting, Microsoft Power BI, People Management.
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Develop and implement data governance strategies for the CMDB to ensure data quality, integrity, and compliance with IT service management standards. Education and experiencePrevious experience (3-5 years) in CMDB management, data governance, or IT service management.
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Ability to collaborate and excel in complex, cross-functional teams involving data scientists, business analysts, and stakeholdersFamiliarity with latest trends in data engineering and data management (APIs, data virtualization, stream data integration, augmented data integration.
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Prior Pharmaceutical or Device industry experience as a MSL or Clinical Trial Liaison giving the candidates a solid understanding of scientific exchange in the context of compliance/ regulated environment and robust experience supporting execution of clinical trials.
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Expertise in SQL Server Management, Azure Data Factory Development, Databricks Engineering, Delta Parquet File Management, and SQL Server Integration Services. Integrate and configure Profisee Master Data Management tools within Azure, focusing on data governance and quality.
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Embedded within Tempus as on onsite researcher, the postdoctoral fellow will have direct access to over 150k de-identified samples with genomic and clinical data, a large organoid repository with genomic and pharmacological screening data, a huge computational environment, and mentorship and collaboration from clinicians, molecular biologists, and data scientists.
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This role will partner with the Contracting team, CIN team and the Clinical teams on evaluating VBC shared savings/risk contracts, incentive programs and distribution, incentive funds flow, calculating and modeling projected financial risk performance (such as risk corridor scenarios, stoploss/reinsurance, feasibility, and scenario analyses.
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The Clinical Trials Unit, directed by Dr. Ian Grant currently works on several interventional and observational studies with subjects that have subjective complaints of memory loss, Mild Cognitive Impairment (MCI), Early Onset Alzheimer's Disease (EOAD), mild to moderate Alzheimer's Disease (AD), Frontotemporal Dementia (FTD), and semantic variant Primary Progressive Aphasia (svPPA.
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Specific responsibilities will include:ANALYTIC REQUIREMENTS:Understanding and being highly proficient at querying a wide variety of healthcare data and related population data (medical/pharmacy claims, behavioral health claims, health care management (HCM) records, electronic medical records (EMR), provider databases (AMA, NPI, DEA, etc.
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PMO lead for onboarding and embedding an ESG Tool, including Carbon Accounting – data sources, aggregation, formatting; process framework and data input controls, change management to embed into ways of workingAssist to design and embed a cost model covering revenue, GP, overhead, fixed costs, and EBITDA to provide multiyear revenue and EBITDA projections to support Sustainability CAPEX/OPEX investments and realize Sustainability Strategy / timely regulatory compliance.
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Agility core practices, Analytical Thinking, Computational Thinking, Continuous Learning, Data Analysis, Data cleansing and transformation, Data Management, Data Sourcing, Data visualization and interpretation, Dialogue enablement, Exposure Management, Machine Learning, Macroeconomics, Market analysis methods, Market Risk Management, Statistics, Trade execution and management, Trading Fundamentals, Sentiment and Trends, Trading knowledge.
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Implemented CI/CD with automated testing in Jenkins, Github Actions, or Gitlab CI/CD Familiarity with AWS Services not limited to Glue, Athena, Lambda, S3, and DynamoDB Demonstrated experience implementing data management life cycle, using data quality functions like standardization, transformation, rationalization, linking, and matching.
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Minimum of 5 years of experience in the structural steel industry, with at least 2 years in a project management or assistant project management role. Utilize Tekla EPM software to manage project data, track progress, and generate reports.
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At least 2 years of experience in information technology (operations, software delivery, access management, microservices), information security (application security, network security, cyber security, data protection), information systems risk management, information systems auditing, or a combination.
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clinical trials data management jobs Title: operations Company: Boston Pharmaceuticals in Chicago, IL
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