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The Rail and Marine Logistics Manager will manage Rail (carload) and Marine modes (inland barge/bulk ocean tanker) planning, execution, operations, and compliance for shipments in RAM (Roehm Americas Region) to achieve Roehm BU service, cost, and sustainability targets.
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Provide guidance on complex compliance matters like anti-bribery, anti-corruption, conflicts of interest, and interactions with healthcare providers, ensuring consistent and practical advice. Juris Doctor (JD) with at least 8 years of experience in legal/compliance roles within the healthcare industry or law firms, including at least 5 years specifically in pharmaceutical company compliance.
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The General Manager (GM) is responsible for overseeing the daily operations of the dispensary, ensuring compliance with state regulations, managing staff, and driving sales to meet business objectives.
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Our spectrum of Global Information Reporting services range from FATCA, CRS, chapter 3 and 61 tax compliance globally, tax form validation services, Qualified Intermediary and Withholding Partnerships regimes, technology development in these areas, consulting services, controversy, risk management and audit readiness for these regimes.
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To request a reasonable accommodation, please call the Luxottica Ethics Compliance Hotline at 1-888-887-3348 (be sure to provide your name and contact information so that we may follow up in a timely manner) or email HRCompliance@luxotticaretail.com.
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Ensure that all activities and duties are carried out in full compliance with regulatory requirements, Enterprise Wide Risk Management Framework and internal Policies and Policy Standards. Working knowledge of lending systems (ACBS, ClearPar, IHS Markit Applications, Loan IQ, payments systems.
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Report suspicions of criminal activity, or any attempt to avoid BSA reporting requirements on the part of customers or employees, to the AML/BSA Compliance Department. Required Experience: Must have attained or worked towards obtaining the ICB Certified Regulatory Compliance Manager (CRCM) certification.
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Understanding of producer data management lifecycle from Pre-Sales, Sales, Underwriting, Compliance, Commissions, Incentives, Marketing, Support Services & Portals, Financials, and Analytics. Ensure the implementation of the data governance program, tools, best practices, and compliance with data standards.
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Under the general direction of the Director of Human Resources, this position is responsible for providing administrative support to the Human Resource Director in the areas of compliance, HRIS administration, recruiting, training and development, event planning, and special projects.
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Provides quality claim handling throughout the claim life cycle (customer contacts, coverage, investigation, evaluation, reserving, litigation management, negotiation and resolution) including maintaining full compliance with internal and external quality standards and state specific regulations.
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Applies litigation management through the selection of counsel, evaluation and direction of claim and litigation strategy. Consults with Manager on use of Claim Coverage Counsel as needed. Skilled in coverage, liability and damages analysis and has a thorough understanding of the litigation process, relevant case and statutory law and expert litigation management skills.
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Understand how to Ensure compliance with industry standards (e.g., HIPAA)Evaluate pre-authorization requests for medical services or procedures. Job DescriptionPosition: HealthCareBusiness AnalystLocation: Parsippany, NJ (Hybrid - need to travel to client place twice in a week)Duration: Full TimeJob Description:Overview: As a Healthcare Business Analyst specializing in claims processing and pre-authorization, you will play a critical role in optimizing the development of our products.
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Actively engages in the identification, selection and direction of appropriate internal and/or external resources for specific activities required to effectively evaluate claims, such as Subrogation, Risk Control, nurse consultants, and fire or fraud investigators, and other experts.
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Collaborate with various functional areas across the organization, including underwriting, claims, risk control, actuarial, legal, marketing, and regulatory compliance in creating products. Provide product-related regulatory and compliance support.
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This includes overseeing the daily global eTMF system related activities relating to clinical study Trial Master Files (TMF), ensuring regulatory inspection-readiness and compliance with applicable laws and regulations.
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compliance job in Dover, NJ
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