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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.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Provides centralized support for document upload and data entry in operational and document management systems (e.g., CTMS, clinical trial and budget tracking, electronic Trial Master File (eTMF), electronic document management system (EDMS) etc.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Develops and modifies hospital policies and procedures for the HIM services such as Medical Coding, Release of Information, Document Scanning and Validation, Data Capture and Reporting, Clinical Document Deficiency Tracking, and File Room Maintenance.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Trial Master File Records Specialist (TRS) Responsibilities. The TRS will provide services onsite (hybrid position) at our Ridgefield, CT location supporting our Trial Master File (TMF) team.
ExpandApply NowActive JobUpdated 14 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.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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NRCS Software and File Management: Gain knowledge of NRCS software (Protracts, Fund Manager, FA Tracker, Conservation Desktop, Document Management System, Excel, NEST). Maintain hard copy and Document Management System (DMS) files.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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At least 8 years relevant clinical research (or related) experience in a biotechnology/ pharmaceutical industry and/or clinical research organization in Clinical Operations and/or a focus on Trial Master File/Clinical Document Management.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Establish and maintain participant files in Document Management System and Protracts. Coordinate paperwork and record-keeping with the USDA Farm Service Agency. Maintain monitoring spreadsheets and enter data into NEST. Navigate CUA process to obtain signatures and upload forms.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Ensure timely close-out of Pfizer Ignite Studies including decommissioning of data & document sharing platforms, overseeing the transfer of study documents from Pfizer to the CRO/ Vendor Trial Master File (TMF) and final TMF transfer to the Pfizer Ignite Partner.
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Expertise in TMF Reference Model and Document management system. The TRS is responsible to provide operational expertise to trial teams and Trial Documentation Service (TDS), oversees the implementation of the TMF strategy for the trial and supports the core trial team in all aspects of TMF management, in inspections or audits and in continuous improvement projects.
$32 - $36 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Research state sales and use tax and other indirect tax issues and document findings. Prepare, review, and timely and accurately file all unclaimed property reports, including mailing of due diligence letters to property owners according to each state's requirements.
$104,000 - $152,350 a yearExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Drives implementation of CDGM initiatives, projects and process improvement activities to enhance clinical document management systems, processes and standards at Novartis. Develop and maintain paper and electronic document processes & standards relating to BD&L projects and Out licensing activities, in compliance with internal and external requirements & regulations.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Proficient with software including but not limited to document management software/iManage, Opus2, Relativity, Lex Machina, Docket Navigator, Westlaw, Lexis, PacerPro, and trial presentation software such as Trial Director.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Work with the audit depart in coordinating file delivery for all audits to GBCI, for FDIC, Accounting firm, Federal Home Loan Bank, Borrower in Custody, and internal audits. Supervises all document preparation, CRA and HMDA on Consumer, SBA and Commercial Loans, post-loan documentation on all loans.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Why LMK: LMK Clinical Research Consulting is a recognized leader in Trial Master File (TMF) document management services and solutions for the life sciences industry. What You Will Be Doing: LMK’s TMF Support Analyst is the Quality Control Expert and ensures accuracy and completeness of all clinical documentation within the TMF. The clinical trial documentation must be consistent with the Trial Master File Specifications, submission/inspection readiness criteria and comply with LMKs (or clients) SOPs and regulatory requirements.
ExpandApply NowActive JobUpdated 9 days ago
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