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And other applicable New Jersey regulatory agencies, including Waterfront Development, Coastal Zone Management, Coastal Area Facility Review Act (CAFRA), Natural Heritage Program (NHP), freshwater and coastal wetlands, watershed and land management (Land Resource Protection), stormwater management, New Jersey Pinelands Commission, former New Jersey Meadowlands Commission, New Jersey Flood Hazard Area Rules, marine sediment and dredging, and the Green Acres Program.
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Maintains knowledge of Federal, State, and other regulatory agency rules and regulations including The Joint Commission, CMS, Medicare, including but not limited to, knowledge of CMS rules regarding Observation status, the 2 Midnight Rule, and Medicare Inpatient Only Procedures.
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Deliverables may include sections of individual protocols consistent with the clinical development plan (CDP), data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications (e.g., investigator brochures, briefing books, safety updates, submission dossiers, and responses to health authorities.
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The Clinical Pharmacist is a licensed professional who is responsible for providing safe and appropriate pharmacy services to Option Care patients in accordance with the policies and procedures of the Option Care, pharmacy practice professional standards, and applicable regulatory entities.
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We are seeking a Consumer Compliance Senior Consultant to be a contributing team member delivering Crowe’s regulatory compliance projects, including compliance audit and testing, program and risk assessments, and regulatory remediation.
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Proven experience collaborating with financial partners to ensure regulatory compliance across various domains including financial crimes, money movement, product obligations, and consumer compliance.
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Regulatory Change Management (RCM):Oversee the review and communication of new or revised laws, regulations, bulletins, and regulatory publications applicable to Property and Casualty Claim adjuster licensing and continuing education.
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Ensure Equipment Compliance: Receive and review revisions to USP, EP, JP, FDA regulatory guidelines. Working knowledge of regulatory guidelines such as FDA, EMA, USP, EP and JP. Excellent computer skills including knowledge of equipment data quality systems.
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As a Barclays US Basel IV Regulatory Capital Vice President (VP), you will account for the calculation & reporting of the IHC’s RWA, Capital, and Single Counterparty Credit Limits and build out of the Basel IV program.
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Description & SummaryA career in our Balance Sheet Management practice, within Financial Risk and Regulatory services, will provide you with the opportunity to help business leaders embed a proactive and dynamic risk management capability and mind set into their corporate business practices.
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Provide legal review, advice, and support on a broad range of legal matters including quality, regulatory, operations, strategic transactions, contracting, licensing, transactional, and general corporate matters across multiple business units in the Cell & Gene Division.
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Serve as a QA representation at key governance meetings whereby GCLP/GLP activities are being discussed (Regulatory affairs, Research unit LT, GRDC etc.,) Effectively interacts with broad range of colleagues in order to establish a globally aligned GCLP/GLP strategy across DS teams.
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Understands and applies all process and regulatory knowledge associated with arbitration and subrogation. Demonstrates knowledge in NJ and in other states and is able to apply regulatory requirements appropriately.
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Provide strategic guidance as the Regulatory Affairs Inflammation subject matter expert on cross-functional/cross-regional sub-teams across development (e.g., Global Development Team, Study Management, etc.
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Monitor legislative and regulatory tax law developments, communicate the effects of these developments to management and the tax team and create strategies to capitalize on changes to taxation legislation.
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regulatory job in Hanover, NJ
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