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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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Join Takeda as a Director, Precision Medicine and Digital Health where you will be responsible for providing strategic guidance and oversight for the delivery of global regulatory strategies to support the development of biomarkers, diagnostic tests, devices, and digital health tools to enhance the value of our products across therapeutic areas.
$165,200 - $236,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Responsible for approval of medical and scientific content of Regulatory, Safety, Scientific Affairs, Medical Affairs and Commercial outputs for assigned therapeutic areas. The Medical Director provides strategic development, planning, implementation and oversight of Phase IV clinical trial programs within the Medical Affairs department for products in the therapeutic area.
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The Data Scientist provides analytical support to Scientific Communications and Medical Affairs & HEOR. This position will report to the Director RWE Analytics and provides exceptional opportunities for career development and growth in a cross-functional and cross-regional environment in the pharmaceutical industry.
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Perform other duties as assigned by the Academic Dean or Vice President of Academic Affairs. Associate Director, Supply Chain and Logistics, Center for Workforce Innovation. Some of the available technologies include Makerspace facilities for podcasting, 3D printing, crafts, and more, a combination of PC and Macintosh computers, scanners, printers, virtual reality headsets, learning hubs, and prayer and meditation rooms.
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The QM Director is responsible for routine reporting to senior leadership and all required external regulatory and accreditation agencies. · Preferably one of the following ASQ Certifications: CMQ/OE Certified Manager of Quality/Organizational Excellence, CQA Certified Quality Auditor, CQE Certified Quality Engineer, CRE Certified Reliability Engineer, CSSBB Certified Six Sigma Black Belt. Strong knowledge of regulatory requirements for cell and gene therapy products, ISO-7 cleanroom, and clinical trials is preferred ( eg.
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Reporting to the Vice President, Government Contract Compliance and Data Strategy, the Director, Quality Assurance and Improvement supports the organization by conducting compliance audits to assist making assessments for process improvements, contract scoring, and compliance.
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Actively pursues effective and efficient operations of his/her respective areas, while ensuring the adequacy, adherence to and effectiveness of day-to-day business controls to meet obligations with respect to operational risk, regulatory compliance risk, AML/ATF risk and conduct risk, including but not limited to responsibilities under the Operational Risk Management Framework, Regulatory Compliance Risk Management Framework, AML/ATF Global Handbook and the Guidelines for Business Conduct.
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Global Regulatory Policy Manager – Liquidity covers a number of key aspects of prudential interpretation, including risk weighted assets (RWAs), capital resources, and the leverage ratio, across a full range of risk areas e.g. credit risk, counterparty credit risk, liquidity risk, securitisation, market risk, etc.
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Reporting to the SVP, Business and Legal Affairs, this person will be primarily focused on supporting the Distribution and Business Development team for Diamond Sports Group that is focused on renewing existing partnerships, building meaningful new partnerships, and helping to secure subscribers and revenue for both Bally Sports MVPD and DTC businesses.
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The General Counsel oversees and manages the universitys legal affairs, providing counsel on a wide range of legal, regulatory, policy, governance and risk management issues that may arise.
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The Platform: The Chief Medical Affairs Office’s Real World Evidence (RWE) Platform is responsible for establishing global scientific leadership and stature through the generation of integrated, end-to-end observational real-world evidence serving all therapeutic areas from proof of concept (POC) trials through LOE for priority pipeline candidates, pipeline supplementation through business development, and marketed inline products.
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Under the direction of the WIC Director and Associate Director, the. Works in close collaboration with the Associate Director, Area Manager, and Training Coordinator to determine the training needs of all the WIC program staff as it relates specifically to CDPH/WIC standards.
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I. Director of Education and Campus Director. Reporting to the Director of Education or Program Chair, facilitate student learning toward the achievement of course and program learning outcomes.
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We currently have an opening for a control room Technical Director at CBS News Streaming! 3-5 years as a newscast director and/or technical director. It is the operator's responsibility to prepare the broadcast through automated protocols (ELC coding by Sony) and technical infrastructure (ELC testing, Viz Director, and Multiplay) for the broadcast.
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director regulatory affairs jobs Company: Metroplus Health Plan in Newark, NJ
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