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Or, ABMGG board certified/eligible for certification in Clinical Cytogenetics and Genomics. Or Clinical Molecular Genetics and Genomics. and assist the Division Director with assay design, feasibility studies, and clinical validation consistent with all regulatory guidelines (CAP, CLIA, FDA.
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The Clinical Coordinator RN provides direct care to patients based on patients' age, developmental level, and priorities. The Clinical Coordinator RN assists in the management of unit personnel, the nursing unit environment, and collaborates with patients, families, peers, physicians and other members of the health care team in the delivery of health care services to all ages of patients.
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Nuclear Medicine Technologist, Clinical and Translation Research Center Position Title Nuclear Medicine Technologist, Clinical and Translation Research Center. The Clinical and Translational Science Institute ( CTSI ) and its Clinical and Translational Science Award ( CTSA ) represent a large NIH Infrastructure grant to support clinical and translational research at the University at Buffalo (UB) and the Buffalo Translational Consortium ( BTC ) partner institutions under the leadership of the Director of the CTSI.
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Proficiency with technical writing, office automation, AutoCAD, MicroStation, or similar software, traffic simulation and modeling platforms including Synchro, HCS, Sidra, Vissim, Vissum. Proficiency with technical writing, office automation, AutoCAD, MicroStation, or similar software, traffic simulation and modeling platforms including Synchro, HCS, Sidra, Vissim, Vissum.
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Tasks may include performing capacity analyses, and assisting with concept development and design, analyzing traffic patterns and modeling, traffic signal design and timing studies, pavement marking design and sign plans.
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The Senior Engineer will also be responsible for managing electrical and control systems for power plants, designing power distribution systems, motor control centers (MCC) with wiring schematics, developing construction specifications, and writing and reviewing equipment specifications.
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The Associate Scientist provides laboratory support in defining optimal particle properties of drug substances as it relates to chemical manufacturing and formulation into pharmaceutical products and is responsible for writing sections of reports for regulatory submissions.
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Manager Revenue Cycle Operations Connecticut Hospital Revenue Cycle Manager Idaho Revenue Cycle Manager Oregon Revenue Cycle Director Connecticut Hospital Finance Manager Connecticut Business RN Manager Perioperative Services Operations New Jersey Manager Patient Accounts New Jersey Clinical Management Consultants Named 28th Fastest Growing Company in Northern California CMC is honored to be named one of the fastest growing private companies in the United States.
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Develop and maintain value sets using national standardized clinical terminologies and code systems (e.g., SNOMED-CT, LOINC, RxNorm). Experience with HL7 standards, including Fast Healthcare Interoperability Resource (FHIR) and Clinical Quality Language (CQL.
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Sr. Integration Architect: (6B) Applicable for OIC, OSB and Gloo API gatewayThorough understanding of software development and/or support methodologies, principles and procedures and related software management toolsExperience using SQL databases and writing SQL queries.
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We are dedicated to providing the highest standards of clinical excellence in order to ensure access for patients to leading providers, while contributing to Stanford University’s well-respected Stanford Hospital and Clinics’ transformation into a broader and more integrated regional health system.
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Education: Graduate from an American Psychology Association accredited college or university with a doctoral degree in clinical or counseling psychology. Operate and manipulate automated systems such as electronic health record, ADS, Essentris, Clinical Information System (CIS) and various other databases, participate in clinical staff Performance Improvement (PI) and Risk Management (RM) functions, as prescribed by the Commander.
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You’ve acquired a minimum of 7 years' Regulatory Affairs experience within FDA regulated, complex Medical Device/Software (SiMD/SaMD) environments, including leadership/guidance on global regulatory strategy for 510K’s, CE Marking per MDD, EU MDR (updating Technical Files), Worldwide product registrations, Design Dossiers, PMA, clinical evaluations, Post Market Surveillance and reviewing Marketing Communication materials for promotional purposes.
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The primary focus of this position is to provide medical services to all eligible beneficiaries within the capabilities normally granted to a Medical Technologist/Clinical Laboratory Scientist (MT/CLS.
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Under the direction and general supervision of the Nurse Manager, the clinical nurse leader utilizes evidence based practices in accordance with the State Nurse Practice Act, policies and procedures of the hospital and as directed by the medical staff.
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writing clinical jobs in Hartford, CT
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