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Has leadership and management responsibility for overseeing the school's financial and budget administration including budgetary targets; human resources/workforce planning and training including recruitment and development program; information technology; office management; faculty affairs; student affairs; scientific/research affairs; clinical affairs; facilities and space management; fundraising; and compliance with applicable laws and regulations.
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This position will work collaboratively with clinical development, pharmacology, pharmacovigilance, clinical drug supply, project management, regulatory affairs, medical writing, clinical data management, and clinical operations.
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As part of the GRA CMC Pharmaceuticals, Oligonucleotides team, you will report to the Executive Director and Head, CMC Regulatory Affairs, Pharmaceuticals. Join Takeda as a Director, GRA CMC Pharmaceuticals, Oligonucleotides where you will lead the GRA CMC Pharmaceuticals Oligonucleotide regulatory team in the development and implementation of global CMC regulatory strategies during development commercialization and post approval LCM stages.
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At least seven years of progressively responsible work experience in higher education administration, with a focus on enrollment management, admissions, and student affairs. The Vice President works collaboratively with the divisions of Academic Affairs, Business Services, and Communications and External Relations to meet college student success and enrollment goals outlined in the college's Strategic Direction and Student Success Plan.
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You will work closely with cross-functional teams, including regulatory affairs, labeling, quality control, and product development, to ensure that our products meet all applicable food safety and compliance requirements, and will support management of any administrative proceedings or litigation related to TreeHouse Foods' adherence to safety regulations, compliance standards and best practices.
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As a member of the Student Affairs senior leadership team, the Dean of Students provides leadership to the Office of Student Accountability & Support, Student Life, Student Engagement & Leadership (Greek Life and Civic Engagement & Volunteerism), and the Student Legal Services (SLS), areas of the Student Affairs portfolio.
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Provide regulatory guidance, general issue management and strategic stakeholder engagement support to Corporate Affairs and business leaders. The Director of State Public Policy role resides within the Corporate Affairs Department and will serve as an expert in state public payer, Medicaid and dual eligible public policy while working with subject matter experts and business units within the Humana enterprise including our Medicare, Medicaid, and CenterWell businesses.
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Abiomed, part of Johnson & Johnson's MedTech, is recruiting for a Senior Regulatory Affairs Specialist. The Senior Regulatory Affairs Specialist will be responsible for developing strategies to obtain FDA clearance or approval of new Class II & III cardiovascular medical devices and improvements to existing devices.
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The Director of State Public Policy role resides within the Corporate Affairs Department and will serve as an expert in state public payer, Medicaid and dual eligible public policy while working with subject matter experts and business units within the Humana enterprise.
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Reports to the VP, Strategy & State Affairs-Corporate Affairs Administration. Assist in the preparation and drafting of testimony, regulatory comments, and position statements sent to legislative and regulatory bodies and other interested parties concerning legislation, policies, published reports, regulations, and statutes governing Medicaid, long-term services and supports (LTSS), and other waiver programs.
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The person in this position will report to the Vice President of Strategy and State Affairs and be responsible for public policy development to inform thought leadership, advocacy, and overall strategic positioning.
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Strong knowledge of state health administrative/regulatory/licensure rules and guidance as well as state health policy. Be an instrumental part of Corporate Affairs at Humana by assisting in the development of Humana's public policy positions for our public payer businesses with an emphasis on Medicaid, dual eligible policy, and future state public health programs.
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As a valued member of the MedTech Product Stewardship organization under the Global Regulatory Affairs organization, she/he can be located at any J&J MedTech site in the US. The role can also be fully remote.
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Job Function Regulatory Affairs. Some of the common product stewardship regulatory programs include ROHS (Restriction of Hazardous Substances), REACH (Registration, Evaluation and Authorization of Chemicals), WEEE (Waste Electrical and Electronics Equipment), CLP (Classification, Labeling and Packaging), Packaging and Packaging Waste Regulation (PPWR), Battery Directive, and others.
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Under direction of the Vice President of Strategy and State Affairs, and with input from enterprise subject matter experts, analyze, draft, and develop state public payer policy positions to support the enterprise’s priorities.
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regulatory affairs jobs Title: sr director Company: Csl Behring
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