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The role of the Clinical Documentation Integrity (CDI) Specialist III is responsible for concurrent and retrospect review and analysis of the medical record to improve overall quality and completeness of clinical documentation.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Author and oversee DMPK/clinical pharmacology related sections of health authority communication documents including regulatory meeting briefing documents, IB, pediatric investigational plans (PIP) and popPK modeling/simulation reports.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Author and review Quality documents such as SOP, OOS/OOT, CAPA and Change Control originated internally as well as at the vendor sites. Generate product release Certificate of Testing (CoT) and associated GMP documentation.
$112,000 - $140,000Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Author and execute study protocols governing bioanalytical studies to support in vivo studies and sample analysis. Author and execute study protocols governing bioanalytical studies to support in vivo studies and sample analysis.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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The position requires the ability to work through each step of an analysis, which may include external visual photo-documentation, electrical test, non-destructive troubleshooting, environmental testing, x-ray evaluation, destructive testing, decapsulation, cross-sections, internal visual photo-documentation, scanning electron microscope (SEM) evaluation, and writing a detailed final report.
$77,000 - $163,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Maintain required documentation according to DDS, DMH, MassHealth, HUD, DPH, CARF, and all applicable regulatory standards as well as Bridgewell policies and procedures. Maintain required documentation according to DDS, DMH, MassHealth, HUD, DPH, CARF, and all applicable regulatory standards as well as Bridgewell policies and procedures.
$21.75 - $22.35 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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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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Performs other administrative documentation and record keeping, such as accountability and statistical reports, billing forms, student intern evaluations, performance evaluations, etc. Ensures clinical documentation is complete and according to departmental standards.
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Key outputs include alignment of the data platform architecture, platform design, data modeling, data integration design, standards documentation, architecture to support partner solutions, and performance aligned with the overall goals and objectives for Apptio's business and vision.
$153,000 - $231,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Demonstrated experience conducting NEPA / CEQA / other analysis and preparation of associated documentation. Comply with regulatory requirements pertaining to the data integrity, documentation, procedures, training, monitoring systems, reporting, and record compliance and retention.
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Responsible for the proper operation and documentation all building systems, to include without limitation, fire alarm, fire sprinkler, security alarm, emergency lighting and signage, emergency egress, building access control, monitoring and recording, fuel distribution, elevators, generators, communications, disposal, sanitary, domestic water, plumbing, electric, heating, cooling, and ventilation.
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Job Summary: The Electrical Analysis - Northeast section of the Materials & Process Engineering Department is seeking an individual to fulfill the role of a Senior Electrical Failure Analysis Engineer.
$77,000 - $163,000 a yearFull-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Your primary role will be to assist the Compliance Manager in maintaining an effective import/export control structure, including operational processes and documentation. Ability to meticulously review documentation and identify discrepancies.
RemoteExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Ensure timely and adequate nonclinical deliveries and safety documentation for clinical trial applications, regulatory interactions, and market registration to global regulatory authorities (e.g. IB, pre-IND, IND/CTA and NDA/MAA.
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The home location will be Lowell, MA. As a Commercial Lending Assistant, you will provide support to Commercial Lending Officers and customers through the entire loan cycle by coordinating pre and post-closing loan documentation, assisting with processing and underwriting tasks, requesting and reviewing loan closing packages, and assisting customers with all banking needs.
Part-timeExpandApply NowActive JobUpdated 5 days ago
author documentation jobs in Wilmington, MA
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