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Medical Center: UH: Clinical Lab (Full-Time, Evening Shift) - Job Summary: The Clinical Lab Scientist 1, under general supervision, operates specialized instruments to conduct clinical lab tests and analyze data from results, to assist physicians with diagnosing medical conditions.
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PhaseForward Inform, Oracle Clinical and/or other clinical data management software desirable;General software skills: MS Access, MS Word, MS Excel, MS Project, Visio, familiarity with medical coding dictionaries, especially MedDRA and WHODRUG.Experience applying best practices in clinical data management programming in the clinical trial environment, including requirements definition and QC plansKnowledge of GCP and other regulations.
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Responsibilities The Trauma Registrar collects, abstracts and enters clinical data for all trauma patients admitted to or evaluated by the trauma service. When it comes to trauma data management, it’s about professionals who can review abstract and validate data for the Trauma Registry, submit data to state and regulatory agencies and work as a liaison between performance improvement functions and the registry.
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Previous clinical laboratory experience as a Medical Laboratory Technician, Medical Technology, Clinical Laboratory Scientist or Medical Laboratory Scientist within a clinical laboratory.
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Performs gating, analyses and scientific review of high dimensional flow cytometry data collected from immuno-oncology clinical trials. Must have at least 5 years of experience in analysis of high dimensional (12+ color) flow cytometry data, specifically with T-cell functional subsets (memory, activation, exhaustion) and/or Myeloid cell phenotyping (MDSC, pDC etc.
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Leverage clinical and data domain knowledge to build data extract, delivery, and transformation processes to meet user requirements. Understanding of data warehousing concepts and experience with data warehousing solutions (e.g., Snowflake, Redshift, BigQuery.
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Utilizes research data to implement clinical changes and the delivery of patient care and member services. Maintains key Relationships with Clinical and Administrative Director peers, Chiefs of Service, other department directors reporting to Assistant Administrators for clinical and operations, regional PCS, AMGAs, community peers.
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Description: Job Summary:Performs pre-analytical, analytical and post-analytical phase testing of all complexities as defined by Clinical Laboratory Improvement Act/Amendment (CLIA) to include specialized tests and analysis in one or more areas of clinical laboratory such as Hematology, Microbiology, Clinical Chemistry, Urinalysis, Immunohematology, Serology, Parasitology and chemical and morphological examinations to obtain data for use in diagnosis and recording laboratory test results.
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Seeking a highly motivated and driven data scientist to join our Quantitative, Translational & ADME Sciences (QTAS) team in North Chicago, IL. The QTAS organization supports the discovery and early clinical pipeline through mechanistically investigating how drug molecules are absorbed, distributed, excreted, metabolized, and transported across the body to predict duration and intensity of exposure and pharmacological action of drug candidates in humans.
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Participates in research studies, including data analysis and reporting, in collaboration with JMCRS, In-Vivo and other members of CMQ.Works with pathologists, Chief of Diagnostic Services, and Biosecurity Officer to investigate unusual clinical cases or cases involving known or suspected infectious disease.
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Required Experience: Degree in epidemiology, biostatistics, data science, clinical informatics, public health, or related fields. The Data Scientist will collaborate closely with product, operations, engineering, data science, and clinicians to provide best in class analysis of oncology care pathways and contribute to technical product requirements with supervision from senior scientists.
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The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results with a high level of proficiency and in accordance with Eurofins Transplant Genomics standard operating procedures.
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Familiarity with data management and visualization tools and collaborating with computational biology to analyze complex data sets emerging from clinical trials. Coordinates appropriate scientific and medical activities with internal stakeholders (i.e. commercial, clinical operations, discovery, statistics, regulatory, etc.
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Clinical Research Coordinator, Norwalk, CT. Responsibilities include; patient screening and recruitment, coordination of care of the research patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board (IRB.
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Position Purpose:The Clinical Supervisor HIV Outreach will oversee the new DHSP Data to Care (D2C) HIV project that utilizes external databases (e.g., Enhanced HIV/AIDS Reporting System [eHARS], HIV Casewatch, etc.
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clinical data jobs Title: operations Company: Boston Pharmaceuticals
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