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Job SummaryThe Director of Regulatory Affairs is responsible for planning, organizing, implementing and evaluating regulatory compliance initiatives to support patient safety and quality and ensure continuous compliance with Federal, State and local regulatory requirements.
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The Vice President for Federal Affairs will work to position the Network as a trusted information source regarding market development, supply chain development, and technological advancement before policymakers and stakeholders, and forge strategic partnerships to advance critical policy or regulatory updates.
$100,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Office of Medical Products and Tobacco Operations in the Office of Regulatory Affairs (ORA), provides advice and counsel to ORA and FDA leaders regarding medical devices and radiological health program operations, including emergency response activities.
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Provides direction and support for Corporate Compliance, including acting as a consultant to the Legal/Sales/Government Affairs/Compliance/Executive Inquiry Teams. Knowledge of NCQA requirements of utilization review, Case Management standards and guidelines, appeal rights and responsibilities, and Regulatory requirements at the state and federal level for health care administration and Carrier standards.
$150Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Comprehensive understanding of applicable standards, methods, processes and practices, business fundamentals, and performance metrics in the specific functional area supported by this position (e.g., asset management, electric or gas operations, customer service, transmission and substation, distribution system operations, regulatory and external affairs, transmission operations and planning.
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Participate in and represent the needs of investigators and leadership in protocol navigation, policy, regulatory affairs, operational committees, meetings or workgroups as well as in other NIH initiatives.
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1 year of experience in a medical/health-related field or in auditing, quality/performance improvement, and/or regulatory affairs required. Under the general direction of the Manager, Quality Systems and in accordance with established procedures, performs a variety of complex and confidential duties to ensure organizational compliance with various state, federal, and industry regulatory agencies for tissue or organ donor records.
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Direct and supervise lobbying efforts to advance legislative and regulatory objectives and protect company's interests from adverse public policy. Reporting to the SVP of Government Affairs, this person would protect and promote Synchrony before the federal government and assigned state governments, while building coalitions and working with allies nationwide.
$150,000 - $250,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Assists chief governmental affairs officer in long-and short-term state legislative agenda oversight to meet University's goals and objectives. Serves as primary contact to respond to state legislative and state regulatory proposals that affect the University and ensures that University acts with a single unified voice, including supporting formal testimony at hearings or other appropriate actions.
$154,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The incumbent will perform program analyses to evaluate efficiency and effectiveness of program practices impacting Native American Tribes, legislative and regulatory issues relevant to HHS and IHS.
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At least 4 years experience in compliance and regulatory affairs, mainly AML/CFT, transaction monitoring, sanctions screening, etc. Act as a point of contact with acquirers, financial partners, and regulatory bodies as appropriate.
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BS + in biology or chemistry, or related field, with industry experience within regulatory affairs, laboratory sciences, quality assurance/control. MM S is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.
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Internally, EPRO works with the Office of Strategic Operations and Regulatory Affairs (OSORA) regarding CMS essential records management. design pattern, lead, maven, php, project architect, senior, software engineer lead.
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Collaborate with cross-functional teams, including R&D, Quality Assurance, and Regulatory Affairs, to ensure product quality and compliance. Certification in relevant quality or regulatory areas.
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Our lawyers and legislative advisors serve domestic and international clients in all areas of corporate and business law, complex litigation, intellectual property, regulatory matters, and government affairs.
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regulatory affairs jobs in Towson, MD
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