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You’ll advise clients on their local and overseas tax affairs, while acting as a strategic consultant related to business analysis, managing indirect taxes, dispute resolution, and global enterprise tax solutions.
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The Department of Defense (DoD) Assessments, Monitoring & Evaluation (AM&E) project is a five-year effort to build a culture of AM&E and establish an AM&E program at each geographic combatant command ( GCC) on behalf of the Deputy Assistant Secretary of Defense (DASD) Global Partnerships (GP) at DoD. The project supports reform of institutional capacity building of partner nations’ ministries of defense with a whole of government approach.
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Support the different functions within the Clinical Team with his/her expertise and leadership (monitoring, data management, biostatistics, medical writing, pharmacovigilance, regulatory affairs) as well as interact with and support Project team members, Clinical Immunology Laboratory, Budget and Planning Functions, Legal and Patent Department, Product Brand Leader and Medical Affairs.
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We specialize in public relations, reputation management, public affairs, brand marketing, digital strategy, social engagement and content strategy. FleishmanHillard, a global integrated communications agency, is seeking a Senior Vice President to serve as a Client Relationship Manager (CRM) and account leader in our Raleigh office.
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This position reports directly to the GVP Global Medical Affairs and will be evaluating, refining, updating, and growing the Drug Safety & Pharmacovigilance function at Kiniksa. The Vice President, Global Medical Safety will be responsible for providing medical oversight for the global drug safety and pharmacovigilance function to ensure proactive and timely benefit-risk assessments of all safety data.
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Foster positive relationships with FDA.Build and maintain a strong, collaborative relationship with all key stakeholders including Commercial, Medical Affairs, Promotion & Compliance, Global Development and other functions key to the success of product development.
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Evidence generation strategy: Collaborate with medical & scientific affairs and global access evidence teams to generate robust evidence supporting the value proposition of our diagnostic products.
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This entails overseeing areas such as manufacturing, quality, process & analytical development, supply chain, and regulatory affairs. Lead, mentor, and develop a high-performing FP&A team supporting Operations, particularly surrounding Novavax COVID vaccine and updated variants, the company s proprietary MATRIX adjuvant, and the Flu-COVID combination vaccine (CIC) and the related expansion of global capabilities.
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Job DescriptionVisa is seeking a lawyer to join its growing Global Regulatory Affairs team. The position will report to a Senior Managing Counsel, Global Regulatory Affairs.
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We help our technology and business teams enable their vision by providing integrated legal guidance and compliance support for global privacy and regulatory affairs matters, including support for information security, incident response related matters and data privacy.
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This role requires strong collaboration skills and partnership with R&D, Global Strategic Marketing, Product Marketing, Regulatory Affairs, Supply Chain, Quality and Finance. RAD is part of Ethicon, Inc. , a global leader in surgery with products and solutions found in almost every operating room around the world.
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Reporting to the Sr. Director, Global Regulatory Affairs, the Senior Manager, Regulatory Affairs provides direct support to Solta operations for their globally distributed products.
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This position is a member of the Medical Scientific Affairs Team and will be fully remote. The Medical Director, Global Scientific Communications for Beckman Coulter Diagnostics is responsible for advancing and facilitating medical communication, scientific dissemination, and external education activities.
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Responsible for developing and implementing global regulatory strategies encompassing clinical, non-clinical and CMC disciplines. Represent Regulatory Affairs in multi-disciplinary teams to establish development and regulatory strategies for early through late-stage development programs.
$200,000 - $284,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The position also has direct interface and activity/strategy coordination with leadership teams in Global manufacturing, Commercial, Regulatory Affairs and Legal and extends to external business partners (TPMs) and regulators.
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