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ResponsibilitiesUnder the general direction of the Associate Vice Chancellor, Strategic Communications and Brand Marketing, the Senior Director, Media Relations and Public Affairs will:-Build and maintain positive, constructive relationships with key contacts across the Chancellor’s Office and the CSU to aid in fulfilling media inquiries.
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Scientific secondary-school diploma with at least 10 years of experience within International Regulatory Affairs. At least ten years of experience within Regulatory Affairs of which at least five in the international context.
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We are looking for a State Government Relations & Public Affairs Lead who is self-motivated, patient-centric, and innovative to join us in our Corporate Affairs Team. This hybrid role, based in Raleigh, North Carolina , will cover the following states: North Carolina, Virginia, West Virginia, Pennsylvania, Ohio, Delaware, and Maryland.
$141,760 - $186,060 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Motivate and guide the professional development of the Legislative Affairs Associate reporting indirectly to the incumbent; The State Government Affairs Manager shall be responsible for leading public affairs strategies geared to support the mission and advocacy goals of JTI USA. This shall include developing and executing state-level advocacy material and plans.
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Proclinical is seeking an (Associate) Director, US Regulatory Affairs, Advertising & Promotion for a large global pharmaceutical company with locations in Georgia, North Carolina and Massachusetts.
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In the role of Senior Director, Regulatory Affairs, you will be responsible for overseeing and directing regulatory activities for new and mature products to ensure alignment and compliance with local and regional registration requirements as well as with company policies.
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The Head of Corporate & Legal Affairs will report directly to the CEO, with whom Cornerstone has had over a decade-long relationship and is a well-respected, collaborative leader with a rich history of working for start-ups and well-established CROs.
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The Regulatory Affairs Specialist coordinates the regulatory activities for life cycle management of marketed pharmaceutical products. Additionally, the role will assist in organizing submission of Advertising and Promotional pieces to FDA. These obligations will also require interactions with the Regulatory Operations team to plan, prepare, and complete accurate and timely submissions to Heath Authorities.
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We are working on a retained search, Director, Global Regulatory Affairs position with a growing pharmaceutical company that is in the areas of rare-disease/immunology/autoimmune diseases. We are working on a retained search, Director, Global Regulatory Affairs position with a growing pharmaceutical company that is in the areas of rare-disease/immunology/autoimmune diseases.
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The lead closely interacts with the Global Marketing, Global and Region Medical, and R&D teams to support registrational trials and provide leadership for global medical affairs sponsored and supported trials.
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The Director, Regulatory Affairs is responsible for assisting with establishing and managing regulatory strategies, life cycle plans, and pre/post regulatory approvals. Establish regulatory strategies and process by collaborating and coordinating with relevant development and CMC team members.
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As Sr Staff Regulatory Affairs Specialist , you will assume a key role in the interpretation and dissemination of global regulations, guidelines, and emerging industry developments that directly influence our business.
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Coordinating with Global Medical Affairs and local cross-functional colleagues (Payer, Marketing and New Product Planning), he/she provides medical leadership to support successful product development, medical launch and product commercialization, while putting the patient first within the Chiesi Values and Behaviors framework.
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The Associate Medical Director, Belotero Lead, provides oversight to the Strategic Direction for the Belotero Portfolio for Global Medical Affairs. Medical Affairs experience. Be familiar with processes and procedures for moving targets from preclinical research through the development pipeline for Belotero.
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Currently seeking a new Global Director of Regulatory Affairs to help spearhead our client's 1st generation PMA submission as well as future supplements and OUS international registries for global commercialization.
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affairs job Title: affairs in Raleigh, NC
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