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Experience with fine arts insurance, knowledge of standard museum loan and registration processes Knowledge of standard best practices and procedures for art handling, transportation, installation, storage, condition reporting, preservation, and basic conservation Proficiency in collections management database software, email, word processing and spreadsheet software, Microsoft Office suite Familiarity AAMD guidelines and archiving methods and practices.
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This involves the development of a control system architecture, selecting the components to be used, detailing schematic diagrams and system documentation, programming controllers (PLC, DCS/Delta V), programming the process visualization (HMI/SCADA), developing databases for archiving/displaying historical system data and implementing/commissioning the control system at the client’s facility.
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Preparing study reports, annual reviews, NIH reports, and Institutional Review Board (IRB) documentation, including reporting of adverse events. Ensuring data integrity through quality assurance checks, and maintaining and uploading data for archiving when required by NIH.
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This involves the development of a control system architecture, selecting the components to be used, detailing schematic diagrams and system documentation, programming controllers (PLC, DCS, RTU), programming the process visualization (HMI/SCADA), developing databases for archiving/displaying historical system data and implementing/commissioning the control system at the client’s facility.
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Assist technologists with picture archiving and communication system (PACS) and electronic medical records (EMR) documentation on an as needed basis. Details Department : Perioperative Care Schedule : 24 hours weekly part time evening shift 3, 8 hour shifts a week.
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Perform and schedule Bi-weekly, monthly, quarterly cleaning of equipment in QC Lab. Support QC documentation, from recording, writing, drafting, reviewing, printing, organizing and archiving as required.
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Work with Quality Systems and CMC team to ensure quality and technical documentation is delivered to the internal archiving system. 5+ years’ experience in GMP Quality or Manufacturing in biopharma/biologics/pharma industry.
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Some highlights include: X-ray, ultrasound, MRI and CT imaging systems, an angiography suite, electronic picture archiving and communication system (PACS) for medical information and file accessibility, a Women’s Center with four labor and delivery rooms, two operating suites and private postpartum rooms, and an Emergency Department with beds and four fast-track beds for patients with less severe conditions.
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Responsible for study completion processes including data lock, study closeout, reporting and archiving of study files, ensuring completeness and continuity of all study data, performing ongoing checks of clinical/translational data that has been entered on the case report forms (paper or electronic) or in reports and assuring archival of appropriate/required documentation.
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Troubleshoots picture archiving communication system imaging archival and issues related to routine data management. Creates and submits documentation for internal continuing medical education programs for Vascular Lab education conferences.
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Review the schedule and weekly narrative to ensure the project is tracking for on-time completion and documentation is in accordance with the MSA / Prime Contract Agreement. Manage all facets of project close-out, including archiving of documents, maintenance and warranty manuals, deficiencies, and warranty work.
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Ensure completeness and proper filing of underwriting and accounting documentation in DMS (Document Management System) as well as physical archiving, where electronical signature is legally not permitted.
$95,000 - $140,000 a year depends on experience (bonuses)ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Clinical Document Governance Management (CDGM) is accountable for strategy and delivery of clinical document management (CDM) systems, processes, standards and operations of CDM services (including Trial Master File management (TMF), clinical submission readiness, record retention and archiving, Good Documentation Practice capability build) across Novartis globally.
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Provide support to the development of an after action report and assistance in archiving the event documentation. Develops pertinent information and provides to the Government POC for communication to varied audiences (e.g., NGA, DoD, NSG, ASG) by extracting and organizing information briefings, read-ahead, and other materials and/or recording and publishing Meeting Minutes with particular attention to detail and quality.
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In addition, this position is responsible for coordinating with all maintenance and engineering departments; updating, maintaining, and archiving current and historical documentation of aircraft and power plant records; monthly coordination and verification of aircraft times and cycles between finance and maintenance computer systems.
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archiving documentation jobs
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