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Present relevant legislative and regulatory measures and Jefferson impact along with relevant Hospital Association summaries during regular Government Affairs team meetings and during standing meetings with Senior VP, Government/External Affairs and Jefferson Leadership team.
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PHMC is proud to be a leader in public health.
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Manage, develop, and implement programming to ensure the TRIO Veterans Upward Bound Program contributes to the educational progress of 160 program participants annually in compliance with University and federal statutory and regulatory provisions.
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Primary Duties: The Department of Pharmacology and Toxicology within Developmental Sciences is seeking an experienced regulatory/project toxicologist and strategic leader to develop and lead the execution of nonclinical safety strategy for gene therapy programs at Spark.
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VetsEZ is seeking a Cloud Data Integration Engineer to join our team and support the Data Migration and syndication (DMS) efforts within the Electronic Health Record Modernization Integration Office (EHRM-IO) for the Department of Veterans Affairs.
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In addition, the Senior Vet Tech is also responsible for preventive health: Rodent animal health surveillance and record keeping; non-rodent physical examinations and record keeping; special treatments and post-operative care; and environmental and equipment monitoring, e.g. anesthesia machines.
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Deloitte Risk and Financial Advisory's Financial Services Industry (FSI) Risk, Data and Regulatory professionals help organizations identify the regulatory changes impacting their business and implement effective and efficient processes to manage regulatory, capital, liquidity and interest rate risks, respond to evolving regulatory environments and implement programs, measures, and tools to help clients with a specific focus on risk, data, and regulatory processes.
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Responsible for ensuring strategic alignment with key internal stakeholders (US medical, commercial, market access, Global HEOR, Global medical affairs). For more information, please visit GSK’s Transparency Reporting For the Record site.
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The NCI/NCTN Senior Regulatory Affairs Start-Up Specialist is expected to resolve, with minimal supervision, regulatory queries, and participate in the initiation of the new study, as well as, communicate transition of the new study to the applicable team Regulatory Affairs Specialist post-site initiation.
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In addition to the responsibilities above, the Clinical Research Coordinator B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board (IRB) documentation through the IRB, including submissions, continuing reviews, amendments, modifications, and adverse event reporting.
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Minimum 3+ years’ experience in risk adjustment coding activities in a Medicare/ACA or provider organization to include RAPS, EDPS, RADV Audits and all CMS/HHS, and other regulatory Guideline required.
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Clinical Research Coordinator B: In addition to the above, the CRC B will establish workflows, pathways, and methods to operationalize protocols, regularly prepare, draft, and submit regulatory correspondences, and mentor/train less experienced research staff in the completion of their duties when required.
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Critical Thinking skills and knowledge within default mortgage servicing and various regulatory and investor frameworks. Critical Thinking skills and knowledge within default mortgage servicing and various regulatory and investor frameworks.
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Provide legal advice on regulatory matters affecting the interests of PGW primarily as it relates to a variety of legal matters which may include but not be limited to regulatory, litigation, municipal, energy and other areas requiring legal counseling and/or assistance etc.
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Interact with artist, record label, management and band tour accountant. Facilitate open communication with the Box Office Manager, staff and all other venue departments. Interact with artist, record label, management and band tour accountant.
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regulatory affairs record keeping jobs Title: regulatory affairs in Philadelphia, PA
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