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15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs/small molecules.
$113 an hourFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Applicants should have a law degree from an accredited law school and a minimum of eight years of relevant experience gained in private practice or as in-house counsel, ideally in the higher education space and with student affairs legal experience.
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This role will manage the back-office operations of the global government affairs function. In this role you will also provide support to Alibaba IGA’s political compliance programs, including but not limited to the EU Transparency in Europe, and the Lobby Disclosure Act (LDA) in the U.S. This role will also provide other related administrative and logistical support for the Head of International Government Affairs for Alibaba.
InternExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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The Senior Scientist I is responsible for oversight of the Scientific Affairs microbiology laboratory operations and performs laboratory investigations for on-market customer support. Oversee Scientific Affairs microbiology laboratory operations, including instrument maintenance, reagent and consumable inventory, SOP development and standard work sustainment and management.
$154,533 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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The network of diplomatic missions abroad is the hallmark of the Ministry of Foreign Affairs and also provides the basis for enabling the Ministry to safeguard and promote Denmark’s international interests in the most optimal way.
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As a member of the Global Medical Affairs team, the Senior Manager, Scientific Alignment will serve as a member of the US Legal, Medical, and Regulatory (LMR) review committee, reviewing US Commercial and Medical materials.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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This role is expected to closely collaborate with multiple teams across Process Development, MSAT, Analytical Development, Regulatory Affairs, Quality and Manufacturing. Author and review plans, protocols, technical reports and CMC sections of regulatory submissions.
$150,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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8+ years relevant experience in quality control, quality assurance, and regulatory affairs at a Class I or Class II medical device manufacturer. Coordinate and organize test data and clinical or scientific reviews in support of regulatory submissions.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Relevant working experience in clinical evaluation, project management, technical/medical/regulatory writing experience, risk management, biomedical/clinical research, regulatory affairs, clinical/quality/R&D engineering, or other related experience.
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The Regulatory Affairs Senior Specialist is responsible for serving as the RA lead on product lifecycle management project teams. Kelly® Science & Clinical is seeking a Senior Regulatory Affairs Specialist for a 1-year contract opportunity with a leading molecular diagnostics company at their headquarters in Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology realm.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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A law firm is seeking an Assistant General Counsel to manage discovery and records related to firm matters, with a primary focus on client file transfers and legal affairs. Experience with relational document review databases (e.g., Relativity) and project management tools.
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As the Director of Regulatory Affairs , you will be responsible for developing and implementing global strategies to secure and maintain market approval for BillionToOne product(s). Regulatory Affairs Certification (RAC) a plus.
$350,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Cross functional partners include R&D, GSM, US marketing, Business Development, Medical Affairs, Clinical Research, Regional HEMA & Marketing, Regulatory Affairs, HCC and Legal. The Director, Health Economics & Market Access for the Robotics and Interventional Solutions platforms, reporting to the Senior Director, HEMA for Energy/Endomech/Robotics, will work in close collaboration with Global Strategic Marketing, Research & Development, Medical, Clinical & Preclinical, and Regional HEMA partners to build and execute fully integrated health economic and market access strategies for the Robotics and Interventional Solutions platforms.
$312,110 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Collaborate with cross-functional teams including biostatisticians, project management, clinical data managers, scientific affairs, medical affairs, and regulatory affairs to ensure timely and accurate delivery of statistical programming deliverables.
$174,182 a yearFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The Sr. Director, Office of Medical Affairs (OMA) is responsible for the oversight of Shockwave Medical, Inc. (SWMI) scientific communications, the investigator-sponsored research (ISR) program, and for the management of medical information on Shockwave Medical products for internal staff and external healthcare professionals (HCP.
$310,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday
affairs job Title: regulatory affairs project Company: Gpac in Mountain View, CA
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