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The Ambulatory Care Nurse Lead will also adhere to practice standards governed by all applicable state federal and regulatory agencies. The Ambulatory Care Nurse Lead will perform duties within the scope of practice ensuring consistency with hospital and WakeMed Physician Practices policies and procedures standards of care standing orders and evidence-based guidelines.
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Knowledge of HIPAA and health care regulatory compliance as they relate to EHR systems and Health Information Exchange (HIE). This position will serve as a Subject Matter Expert on clinical data and electronic health record systems and will act as a liaison between health care providers and the HIE to improve quality of the data sent to the HIE. This position will involve use of Mirth Interface Engine, Intersystems HealthShare Health Insight, HealthShare Clinical Viewer, and SAS technologies in support of the North Carolina Health Information Exchange Authority.
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Work with project teams and plant personnel across our exterior building products manufacturing segments to ensure environmental compliance at new and existing facilities, including oversight and technical/regulatory support for air, wastewater, stormwater, hazardous waste, spill prevention and emergency response regulatory activities.
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Maximus will comply with regulatory minimum wage rates and exempt salary thresholds in all instances. Proven experience with Solarwinds, Microsoft SCCM/MECM, ServiceNow, Infoblox DDI (or related DDI platform), Atlassian Suite, and M365 tools.
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This role functions within the RBC Bank Office of Technology Risk & Controls team which holistically is responsible for establishing, enhancing and sustaining an effective Risk and Control environment for IT in accordance with RBC Bank’s IT Risk Management Frameworks/Policies/Standards and US Regulatory Compliance.
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This position requires a deep understanding of pharmaceutical manufacturing principles, process engineering, and regulatory compliance. Knowledge of regulatory requirements and quality systems in the pharmaceutical industry.
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Provide regulatory review for reporting activities required by EU MDR (i.e. post-market surveillance, reporting, etc. The Sr. Regulatory Affairs Specialist (SRA) will develop US, EU, and Canada strategies, assessments and submissions for complex projects and review issues related to regulatory documents, investigations, product development planning and regulatory agency interaction.
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Support the Public affairs team’s writing and material production to educate internal and external stakeholders on the impacts of current and proposed regulatory and legislative changes. Ideal candidates will be enthusiastic team players who have experience in political campaign communications, public relations, advocacy and/or government relations and are creative, organized, and used to working with multi-department teams to bring projects to fruition.
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CPS Solutions, LLC helps clients tackle a variety of complex issues, such as operational efficiency, rising drug costs, regulatory & compliance, 340B, and specialty pharmacy strategy. About CPS Solutions, LLC: Founded nearly 50 years ago and employing over 2,500 clinical, regulatory, and operational pharmacy professionals, CPS Solutions, LLC, is one of the nation’s largest providers of pharmacy services to more than 800 hospitals and healthcare facilities nationwide.
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Follow regulatory requirements including those pertaining to the Bank Secrecy Act (BSA), Anti-Money Laundering (AML), Customer Identification Program (CIP), and OFAC to assist in the identification, detection and determent of money laundering and other unlawful activities, as well as regulations pertaining to lending and consumer compliance to include fair lending laws.
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Q2 is seeking a Senior Corporate Counsel that will support the General Counsel and Deputy General Counsel in a broad range of complex legal matters for Q2 Software and its affiliated entities (“ Q2 ”) including assisting them with managing legal, compliance, and regulatory issues for a complex, publicly traded financial technology company.
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Learn to perform FAI/CVI (Annual) (First Article Inspection - Commercial Vehicle Inspection) inspections on all fleet vehicles including tractors, trailers, converter dollies, light-duty vehicles, and any other company-owned equipment under the guidanceof fleet technician II & III or fleet supervisor or manager in accordance with all federal, state and local legal and regulatory agencies.
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Accurately complete patient accounts based on departmental protocol, policies and procedures, and compliance with regulatory agencies, to include but not limited to pre-admission, admission, pre-registration and registration functions.
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Subject matter expert (SME) level of knowledge working with clinical data, electronic health record (EHR), HL7 v2 (primarily ADT data), and C-CDA me. Subject matter expert (SME) level of knowledge working with clinical data, electronic health record (EHR), HL7 v2 (primarily ADT data), and C-CDA messages.
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Follow all laboratory policies and Standard Operating Procedures (SOPs) in accordance with regulatory guidelines set by the Clinical Laboratory Improvement Amendments (CLIA) and the College of American Pathologist (CAP) Laboratory Accreditation Program.
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regulatory job Company: Jobget in Cary, NC
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