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About you: You have a strong aptitude for querying data sets from heterogeneous sourcesboth structured such as SQL Server, MYSQL and Vertica and unstructured like Excel,CSV using simple and advanced SQL You have hands-on experience with Databricks (Spark), the AWS ecosystem including (S3, Athena, Glue, Lambda, IAM, EC2) You have hands-on experience in building large-scale distributed applications, including streaming and Batch pipelines and processing petabytes of data.
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Sodexo is seeking a Registered Dietitian for a Clinical Nutrition Manager position at Cooper University Hospital, located in Camden, NJ. This 670-bed hospital is South Jersey’s only level one trauma center.
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Clinical Research Coordinator will recruit and perform study visits, enter data, resolve queries, facilitate specimens collection and shipment. Clinical Research Coordinator B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board (IRB) documentation through the IRB, including submissions, continuing reviews, amendments, modifications, and adverse event reporting.
$37,220 - $65,521 a yearFull-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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Ability to effectively convey clinical guidelines and epidemiological data to various audiences. o Knowledge of and experience with biomedical HIV prevention approaches, specifically PrEP; clinical experience desirable.
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The position's role focuses on provision of comprehensive statistical support, specifically related to design and implementation of studies, collection and management of study data, patient safety monitoring, statistical data analysis, and interpretation of statistical data for preclinical studies, clinical trials, retrospective studies, epidemiological, and bioinformatics-related research, and summarization and reporting of study results for professional conferences and publication.
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The CRU Regulatory Affairs Office seeks a full-time Regulatory Affairs Veeva Quality Assurance Specialist to participate in the review and migration of Phase I-V clinical trial investigator site files to the Veeva SiteVault platform.
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Work with IT Director, clinical staff, and Director of Operations to support Esperanza's data strategy. Working in collaboration with IT Staff, clinical staff, and other departments, this position will deliver data-driven guidance to support the organization's goal of providing executive leadership, clinical providers, and support staff with actionable intelligence reporting related to the performance of the quality measures established for our EMR. Candidates must have experience using data mining tools, statistical analysis, and reporting tools.
$60,000 - $78,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Clinical Pharmacist Specialist is responsible for assisting in the planning, organization and direction of clinical pharmaceutical services to achieve high quality standards of care in pharmacy services related to specific areas of clinical expertise.
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3+ years of experience with data applications (Spark, Presto, Hive, etc)3+ years of experience in designing and building ETL pipelines to process data at scale3+ years of experience with NoSQL implementation (AeroSpike, DynamoDB, etc)3+ years of experience with a public cloud (AWS, Microsoft Azure, Google Cloud)3+ years of experience with CI/CD tools such as Jenkins or AWS CodeBuild, Terraform, etc.
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Designs, develops, and implements ETL/ELT processes using Azure Data Factory, Synapse pipelines, Databricks Notebooks, Event Hub to build integrations from Saas sources such as Service Now, Workday, Dynamics CRM, and Eloqua.
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Tech will include; Embedded Systems, Wireless Data Transfer, MCU, PCB, iOS / Android. Core technology includes - Embedded Systems, Wireless Data Transfer, MCU, PCB. Tech will include; Embedded Systems, Wireless Data Transfer, MCU, PCB, iOS / Android.
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Assist with testing and data validation activities involving PwC, DSC, RJW, Celigo, and Orderful. Proven ability to manage testing and data validation processes with multiple stakeholders, including PwC, DSC, RJW, Celigo, and Orderful.
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Leading the design, build, migration, and testing of OneStream for multi-dimensional data models (dimensions, hierarchies, attributes); input template and report build; Data Integration and Extract Transform and Load (ETL) concepts; understanding of calcs (allocation, top-down spreading, currencies); and, workflow, data permissions and security.
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As a Trauma Registrar, you must be comfortable with interpreting medical clinical data and with advanced computing and data analysis skills. As a Trauma Registrar RN, you will be responsible for overseeing the trauma registry database to include patient identification, abstraction, coding and entering data; retrieval and presentation of registry data for quality improvement, education and research.
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Through the efforts of strategic partners Sage Bionetworks and cBioPortal, the registry aggregates, harmonizes and links clinical-grade, next-generation cancer genomic sequencing data with clinical outcomes obtained during routine medical practice from cancer patients treated at these institutions with the goal of improving clinical decision making and catalyzing clinical and translational research.
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clinical data jobs Title: operations Company: Boston Pharmaceuticals in Philadelphia, PA
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