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The Document Validation Specialist position exists to index documents using various modules into Content Manager, performing post funding audits on funded deals, maintaining, and delivering original documents, and troubleshooting unidentified/missing loan processing mail.
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As a CGS Mandarin Document Reviewer you will play a key role in supporting various aspects of the company's litigation portfolio including eDiscovery activities, workflow management, and litigation support.
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Serves as a developer and administrator for a large and growing implementation of Hyland OnBase, an enterprise document management system housing millions of documents essential to the operation of the university.
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In addition, Document Processing Specialists are responsible for communicating all issues that impact the quality or timely completion of the production process to the Imaging Supervisor or Regional Director of Operations.
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Document Control Specialist $66,560.00 - $83,2000.00 $32.00 - $40.00. AGS has an IMMEDIATE opening for a Document Controls Specialist. 3-5 years previous Document Specialist, Administrative Assistant or Office Assistant experience.
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The Senior Manager/Manager Regulatory Document Submissions will report to the Director of Medical Writing, Regulatory. Senior Manager/Manager Regulatory Document Submissions. Utilizing its proprietary AOC platform, Avidity demonstrated the first-ever successful targeted delivery of RNA into muscle and is leading the field with clinical development programs for three rare muscle diseases: myotonic dystrophy type 1 (DM1), Duchenne muscular dystrophy (DMD) and facioscapulohumeral muscular dystrophy (FSHD.
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The Document Control Manager, reporting to the Associate Director, Document Management and Training, will assist in the daily management of document control and training program activities to ensure GxP compliance.
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The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the BMS Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review and system reporting.
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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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Position Reports to Jenna Walker – Associate Director, QA Training & Document Control. Cell Therapy Document Control Specialist (WA) Cell Therapy Document Control Specialist.
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Provides oversight on key Health Information Management (HIM) services provided at a DHS hospital, such as Medical Coding, Release of Information, Document Scanning and Validation, Data Capture and Reporting, Clinical Document Deficiency Tracking, and File Room Maintenance.
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The Document Control & Quality Specialist also assigns change implementation tasks, enters information into the QMS, and releases change requests for use within the organization. [Contract] Document Control & Quality Specialist at Liv Labs (United States) | BEAMSTART Jobs.
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This may include the set-up, organization, and standard content management for various document types as well as overseeing and managing the publishing and archiving activities for global clinical documents managed by GMW. The Medical Technical Writer serves as the interface between GMW and Global Regulatory Operations.
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Deep understanding of drug development process, international drug approval procedures and standards (e.g., ICH-E3, ICH-E6, eCTD) and industry-wide standards in clinical document management (e.g., DIA TMF reference model.
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AECOM is looking to fill multiple full time Document Validation Specialists (DVS) to support a contract with the Federal Emergency Management Agency (FEMA) Public Assistance (PA) Program supporting FEMA’s four Consolidated Resource Centers (CRC.
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document job Title: clinical research associate Company: Parexel
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