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The FRM will need to coordinate cross functionally within Field Sales, Marketing, Market Access, Public Affairs, State & Government Affairs, Trade, and Specialty Pharmacy Account Management.
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Minimum of three years of experience working with college students in a co-curricular environment through civic engagement, student affairs, or academic affairs. Programs include but are not limited to NJIT's diversity dialogue series, heritage month-long celebration programs, awareness day programming, student organization events, identity-based student organization retreat, heritage month programs, MLK Celebration Program, etc.
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They must encourage teamwork to achieve fundraising and external affairs objectives that support the organization's mission. Development Associate, Major Gifts Officer, Mid-Level Giving Manager, Director of Grants Management, Director of Marketing, and the Director of Education Services.
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Demonstrates knowledge of post-educational, private sector work in the financial services or bank regulatory areas required, including: Prepayment, credit risk, fair lending, default, Basel or fair lending modeling/modeling validation, advanced statistical and/or econometric modeling techniques and complex Excel-based spreadsheet models Statistical modeling assessing strengths and weaknesses.
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Primary source verification: NJ Division of Consumer Affairs, Board of Nursing; University Hospital's designated Background Check Company. The Radiology RN (Nurse) is a Critical Care RN and delivers general nursing care to patients in all areas of the Radiology/Imaging and Pain Management Departments including: Vascular and Neurovascular Angiography, Pain Management and Diagnostic Imaging areas of Ultrasound, Computed Tomography (CT), Magnetic Resonance (MRI), X-ray, Nuclear Medicine and Mammography.
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At minimum 10 years' experience in the pharmaceutical industry in Biologics/Research & Development/Regulatory Affairs. Ensure strategic regional regulatory input which is in consideration of the commercial strategy and is provided into global regulatory teams and that the Regional Regulatory TA Team supports the Global Regulatory Affairs (GRA) vision of excellence, good scientific practice, integrity and compliance with regulatory standards.
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Maintenance of Regulatory Affairs product files and ensure compliance with regulatory requirements. Must have a minimum of 5 years of IVD Regulatory Affairs experience.
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Job DescriptionRole SummaryThe Associate Director, Healthcare Quality Improvement is a role within the Global Professional Relations and Independent Medical Education (gPRIME) team of Global Medical and Scientific Affairs (GMSA) that is primarily responsible for supporting Our Company’s collaboration with key external healthcare quality organizations and engagements with professional medical societies on ways to improve healthcare quality and guideline-concordant care.
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Clinical supplies, biologics, vaccines, electronic batch record review, batch record, cGMP, SOPs, specifications, labeling, regulatory submissions, SAP, Trackwise, Midas, Veeva, QMAS, QA, Quality Assurance.
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Collaborating with cross-functional teams including Clinical Operations, Regulatory Affairs, Pharmacovigilance, and Medical Affairs to ensure alignment of medical objectives with broader organizational goals.
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The sections are: Community Affairs, State & Elections, Consumer Affairs Counseling, Education and Higher Education, Employment Counseling and Labor, Health and Human Services, and Law & Public Safety.
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Work with R&D scientists, regulatory, commercial, and management teams to provide quick and accurate IP and other legal advice on all aspects of the Hatch-Waxman Act, including the timing of product approvals and launches.
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The Quantitative Pharmacology and Pharmacometrics (QP2) department drives model-informed drug discovery and development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions.
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Participates in regulatory and legislative affairs for assigned states, including serving on boards and bureaus. The Regional Vice President leads the execution of the CORE (middle market and small commercial) businesses operating plans, new business development, retention, and distribution management.
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Collaborating with the Phillips 66 State Government Affairs Manager by tracking and engaging in state legislative activities and bills that may influence refinery business, recruiting refinery personnel participation as appropriate.
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regulatory affairs registration jobs in Kenilworth, NJ
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