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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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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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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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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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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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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.
$20 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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2-5 years of experience in regulatory affairs within the pharmaceutical or biotechnology industry, with a focus on regulatory operations. As the Regulatory Affairs Operations Specialist, Ad/Promo, you will play a pivotal role in ensuring regulatory compliance and operational efficiency within our organization.
$81,000 - $99,122 a yearFull-timeRemoteExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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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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Eneral Statement of Duties and Responsibilities The DCAMM Director of External Affairs reports to the Chief of Staff and serves as an important member of the Executive Office team, helping DCAMM contribute to the Administration’s policy and goals related to decarbonization and housing, as well as access and opportunity for underrepresented populations, in addition to supporting the core mission of the agency in real estate, planning, design and construction.
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This person will oversee Medical Affairs including development of strategies and supporting execution for sub-functions (Strategy and Operations, Field Medical Affairs, Medical Communications, Value Evidence and Strategy, and Patient Advocacy.
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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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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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Brightcove is looking for a Vice President, Business & Legal Affairs. DescriptionResponsibilitiesThe Associate Vice President (AVP), IT Procurement - Enterprise Procurement & Supplier Management reports to the Chief Procurement Officer, the Associate Vice President - IT Procurement is accountabl.
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Market research studies are paid engagements Ivy Exec conducts with clients to get feedback on certain topics.
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Job title: Global Regulatory Affairs LeadLocation: Cambridge, MA or Bridgewater, NJAbout the jobThe Global Regulatory Affairs Lead (GRL) is the fully accountable decision maker for the development & execution of creative, thoughtful, and robust global regulatory strategies for their products in Sanofi’s diversified portfolio in order to meet corporate and business objectives.
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Title: affairs Company: Turnstone Biologics in Waltham, MA
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