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MedPro is one of the largest recruiters of therapists and nurses from outside the U.S. MedPro currently has contracts with numerous organizations to service a multitude of facilities in the U.S. The company counts among its clients prominent healthcare facilities and organizations such as the Department of Veterans Affairs,HCA, University of Miami Hospital, and Tenet Healthcare.
$2,678 a weekFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Work closely with the Government Affairs Managers to monitor and respond, as appropriate, to all legislative and regulatory proposals affecting JTI USA's business operations. The Legislative Affairs Manager will collaborate closely with our Federal and State Government Affairs Managers to develop impactful advocacy materials, identify key stakeholders, and effectively communicate our positions to those stakeholders.
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The Vice President provides leadership to all areas within Student Affairs including Residence Life, Student Activities, Campus Police/Security, Counseling Center/ADA Compliance, Counselors, and Intramurals.
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The Sterilization Technician ensures regulatory compliance, assists in inventory management, and may serve as an advisor to other TriMedx personnel on technical matters concerning specialty equipment.
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Assist Category Managers to Identify and assess potential risks in the supply chain, such as disruptions, geopolitical issues, natural disasters, supplier financial instability, regulatory changes, and other external factors.
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Master’s degree in International Studies, Higher Education and Student Affairs, Counseling, Social Work, Foreign Language, Communications, or related field. Stay abreast of regulatory changes impacting F-1 and J-1 students and scholars and of procedural changes at USCIS , SEVP , ICE , DOS , and other governmental agencies impacting international students and scholars.
InternExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Collaborate across the organization in Regulatory Affairs, Clinical Operations, and Patient Engagement. Clinical research neurologist, investigator, neurologist, principal investigator, PI, neurology, part-time, clinical trials, clinical drug development, oversight, leadership, FDA, GCP, safety, assessment, regulations, medical license, clinical research, on-site, Raleigh, RTP, NC, North Carolina.
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Supporting formulation development steward new technical molecules into the country, working closely with regulatory and marketing members, providing method development for various types of agricultural active ingredients.
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ResponsibilitiesUnder the general direction of the Associate Vice Chancellor, Strategic Communications and Brand Marketing, the Senior Director, Media Relations and Public Affairs will:-Build and maintain positive, constructive relationships with key contacts across the Chancellor’s Office and the CSU to aid in fulfilling media inquiries.
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Support Bandwidth’s public policy advocacy efforts at the Federal Communications Commission, state public utility commissions and international regulatory authorities on issues related to voice communications, telephone number administration, CPaaS, UCaaS, CCaaS, intercarrier traffic exchange, emergency calling and SMS/MMS services.
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B.Upholds all health care system/organizational policies and procedures and clinical competencies put forth by this job description and professional association including legal, regulatory and accreditation requirements and standards ensuring by way of example, such goals as TJC Patient Safety Goals and Wellstar Health Systems’ safety absolutes C.Participates in data collection, poses relevant clinical questions to advanced evidence-based practice.
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Alignment with the CCS GRC, Business Unit Risk Management, Technology Risk, Truist Audit Services and Regulatory Relations, as well as the needs of the lines of business that they support. Understand multiple approaches to regulatory compliance and control effectiveness design.
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Provide general advice on intellectual property issues, including trademark, copyright and patent issues in coordination with Global Trademark Counsel and Patent Affairs. Provide FDA regulatory advice to the product marketing teams by participating in Promotional Review Committees for the Company's products.
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They are accountable for execution of all applicable risk programs (Credit, Market, Financial Crimes, Operational, Regulatory Compliance), which includes effectively following and adhering to applicable Wells Fargo policies and procedures, appropriately fulfilling risk and compliance obligations, timely and effective escalation and remediation of issues, and making sound risk decisions.
$179,200 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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6 months to 5 years of experience in Regulatory Affairs of a Consumer Products Company with working knowledge of U.S. FDA labeling regulations as published in 21 CFR Parts 1-199. Vaco Boston has partnered with our client to hire a Regulatory Specialist to join their team.
$39 an hourRemoteExpandApply NowActive JobUpdated Yesterday
regulatory affairs jobs Title: travel in Raleigh, NM, Wyoming
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