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The Executive Director, Regulatory Affairs will develop and execute global regulatory strategic and tactical guidance for the development of innovative new drugs in rare disease ensuring fast to market global product registrations, product promotion, maintenance of products and processes in regulatory compliance with local regulations.
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Proactively anticipate and research issues related to areas such as state and local government affairs, regulatory filings, grassroots and political action activities, public affairs, and economic development.
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Regulatory Compliance: Familiarity with relevant regulations and guidelines governing credit data, such as CCAR, CECL, and Basel III. Credit Risk Management: Knowledge of credit risk principles, methodologies, and regulatory requirements.
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Stakeholder Collaboration: Work closely with other departments, such as Technology, finance, modeling, regulatory reporting, Enterprise Data Governance and risk management, to ensure data initiatives are integrated and aligned with business objectives.
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ADARs will also be required to coordinate and communicate cross-functionally within NPC (e.g., Patient Support Center, Customer Engagement, Marketing, Market Access, Public Affairs, State & Government Affairs, Trade, Specialty Pharmacy Account Management, and other applicable third-party affiliates.
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Maintain current knowledge of relevant Quality System Regulations and other regulatory requirements related to research and development (product development, design and safety) to ensure compliance in all research, data collection and reporting activities.
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ADARs partner closely with other Novartis Pharmaceuticals Corporation (NPC) field associates, including Customer Engagement (Sales) and Market Access, representing NPC with the highest integrity in accordance with NPC Values and Behaviors.
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Proven experience in the medical industry (clinical, scientific communications, medical affairs, medical education, product management, product development, R&D, medical sales, or field clinical engineering) and in an FDregulated environment preferred.
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As a Regulatory Policy Advocate, you will be responsible for assisting the Director of Policy in their work to analyze, develop, communicate, and advocate for CEE's policy positions to the Minnesota Public Utilities Commission (Commission), the Department of Commerce, and in other public venues.
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7+ years of experience working with the state Legislature, the Executive Branch, municipal government officials, government relations, public policy, advocacy, government affairs, or campaigns. The Vice President, State Government Affairs will be part of the UHG External Affairs organization, responsible for working with colleagues across External Affairs and the Company to develop and implement strategies on the company's declared state government advocacy, growth, relationship and reputational priorities and overall business advancement initiatives with key state policymakers.
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As an AML Investigator, you will conduct enterprise-wide investigations identifying unusual activity and preparing Suspicious Activity Reports (SARs) to be filed with Financial Crimes Enforcement Network (FinCEN) as well as writing and preparing cases that result in No SARs. An AML Investigator should have a basic understanding of AML/BSA laws and regulations, the financial services industry, and regulatory trends that impact their assigned line of business.
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Whether specializing in law, government affairs, employee relations, risk, compliance, ethics, security or food safety, we use our expertise and influence to advocate for Target, support Target’s business and mitigate risk for the company.
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Support retention efforts in other Student Affairs departments including Esports, Women's Initiatives, Housing and Residence Life, Career Services, Student Success, and the Learning Commons as needed.
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The Director of Regulatory Affairs and Customer Compliance is responsible for overseeing and providing leadership for all regulatory and export compliance matters within the MFI Integrated Supply Chain.
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Completes clinical documentation in compliance with The Emily Program and Veritas Collaborative policies and regulatory standards. Completes clinical documentation in compliance with The Emily Program and Veritas Collaborative policies and regulatory standards.
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regulatory affairs jobs Title: affairs manager Company: Gpac in Robbinsdale, MN
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