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The Associate Medical Director (AMD), under the direction of the Director of the Office of Clinical Affairs (OCA) or his/her designee, is responsible for providing clinical expertise to OCA and EOHHS program staff.
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The Director of Quality and Regulatory Affairs is responsible for developing and implementing the long range regulatory and compliance strategy by leading and directing the organizational development, processes and activities required to support the Biofourmis remote patient monitoring platforms and pharma partnerships on a global basis.
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Role Summary The Executive Assistant will provide high-level administrative support to the Head of Corporate Affairs and Head of Patient Office within Servier Pharmaceuticals. We are a commercial stage, privately held pharmaceutical company, based in the U.S. Currently, we have four medicines approved in acute lymphoblastic leukemia (ALL), acute myeloid leukemia (AML) and cholangiocarcinoma (CCA.
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ResponsibilitiesThe Assistant Dean of Clinical Affairs for the School of Nursing will work with the healthcare clinical facilities located in the Northeastern University Network to include the Boston, Burlington, and Charlotte campuses as well as those affiliated with our satellite programs to establish and maintain sites for student placements in clinical and practice settings at the prelicensure and graduate levels.
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We're hiring for a Government Affairs Manager who will be responsible for implementing strategies to advance the company's legislative and political agenda. We're hiring for a Government Affairs Manager who will be responsible for implementing strategies to advance the company's legislative and political agenda.
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Lantheus is an entrepreneurial, agile, growing organization that provides innovative diagnostics, targeted therapeutics, and artificial intelligence (AI) solutions that empower clinicians to find, fight and follow disease.
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Then AstraZeneca might b Regulatory, Regulatory Affairs, Director, Strategy, Global, Senior, Business Services. Do you have expertise in, and passion for, Regulatory Affairs? Then AstraZeneca might b Regulatory, Regulatory Affairs, Director, Strategy, Global, Senior, Business Services.
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10 years of relevant professional experience, including at least 3 years in Regulatory Affairs in a U.S. advertising and promotion role. Collaborate with colleagues in Commercial, Medical Affairs, Legal, Compliance and other expertise areas in creation of promotional and disease awareness communications, field training materials, and materials and communications used in scientific exchange, for assigned product(s.
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We're looking for an Associate Director Regulatory Affairs CMC , working in Pharmaceuticals and Medical Products industry in Cambridge, Massachusetts, United States. Manages timely regulatory submissions that involve CMC components including CTAs/INDs, NDA/MAA, and agency meeting packages.
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At least 10 years’ experience in Regulatory Affairs, with direct experience in Labeling and Advertising/Promotional review. Create/revise SOP’s and Work Instructions as applicable, to ensure high performing regulatory operations and effective review processes.
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You’re the right fit if you have the following:You acquired a minimum of 5 years’ experience in regulatory affairs within the FDA regulated, global medical device industry. JOB DESCRIPTION Job TitleRegulatory Affairs Program ManagerJob DescriptionAs a Regulatory Affairs Program Manager, you will be an important member of the Philips Regulatory Affairs Centralized Services Team, committed to improving billions of lives worldwide.
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Director, Regulatory Affairs. serves as a strategic regulatory leader for assigned drug development programs and uses extensive knowledge to advise project teams on regulatory requirements to drive successful global development strategies.
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Work extensively with Alexion leaders across multiple departments including Early and Late R&D, RWE Generation, Global and In-Country Medical Affairs, Commercial, Public Affairs, Patient Advocacy, Market Access, and Clinical Operations to optimize Alexion interactions with the scientific societies and identify expanded areas for collaboration.
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Health + Wellness - Medical, Dental, Vision and Life Insurance along with additional wellness support. You balance multiple projects and meet deadlines in a fast-paced, rapidly changing environmentYou have demonstrated experience in developing both long- and short-term advocacy strategies and tactics along with coalition building with diverse interests to advance policy priorities.
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The Legislative Affairs co-op will report directly to the Chief of Intergovernmental Affairs, and work as part of the Legislative Affairs Team to support their ongoing projects. Learn day to day activities of a Legislative Affairs/Intergovernmental operations.
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Title: affairs Company: Turnstone Biologics in Waltham, MA
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