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As The Focus Of This Internship, We Would Like To Study The Potential For How Generative AI Can Be Used In The Drug Development Lifecycle To Accelerate The Approach To Areas Such As Regulatory Filings, Generation Of Real World Evidence, Clinical Trial Documentation And Audits.
$10,120 - $12,170 a yearInternExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Work across a variety of functions involved in drug development, such as preclinical, clinical, regulatory, biostatistics, and medical affairs. As a Clinical Pharmacologist, the Associate Director/Director will be responsible for designing, conducting, and analyzing clinical pharmacology studies, as well as providing expert advice on pharmacokinetic and pharmacodynamic aspects of drug development and regulatory submissions.
$125,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Work closely with the Head of Scientific Affairs & Strategic Partnerships and Scientific Affairs team to produce rapid, thoughtful responses to content-related requests from across Pfizer Oncology (CSO, Medical strategy, BoD, Investor Relations, colleagues, etc.
$191,300 - $318,800 a yearFull-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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The Microsoft Corporate, Legal and External Affairs (CELA) organization seeks a highly motivated, experienced Legal Counsel attorney to join the Governance, Training, and Culture (GTC) team in CELA’s Compliance & Ethics organization.
$101,200 - $213,200 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Principal Regulatory Affairs Specialist will prepare comprehensive regulatory strategies for complex new devices and post market changes within our Ultrasound business.
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To that end, the US Government Affairs (USGA) team is looking for a Program Manager to assist members of the State Government Affairs (SGA) Industry team by providing related programmatic support and project management.
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The Sr. Regulatory Affairs Specialist assists with development, management, and implementation of regulatory strategies to support new and existing Class I and Class II ophthalmic medical devices.
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Director of Government Affairs and Public Policy Modern Hydrogen Woodinville, WA - Full Time – Remote We are seeking an accomplished, enterprising government relations leader with over 15 years' experience driving policy transformations through bipartisan political channels and public-private partnerships.
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The Associate Dean also works closely with campus stakeholders, such as Basic and Transitional Studies (BATS), Student Affairs, Workforce Education, and the Office of International Education and Global Initiatives to implement new and continuing program initiatives, such as international clinical experiences and exchanges.
$124,346 - $165,795 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Deliver advice on a wide range of regulatory compliance topics and programs, including green chemistry federal and state reporting and disclosure requirements, conflict minerals, state minimum pricing, motorized vehicles, contractor licensing, independent optometrist matters, third party insurance agreements, advertising in Puerto Rico, and the USDA Supplemental Nutrition Assistance Program.
$110,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Our client is an environmental consulting and construction firm that designs and implements sustainable environmental solutions, including solid and hazardous waste management, landfill gas, site remediation, renewable energy, and regulatory compliance.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Drive operational preparedness for regulatory requirements and collateral management functions. The Trade Operations Manager will have a strong knowledge of fixed income securities, FX, derivatives, collateral management, vendor management, and portfolio system flows.
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Familiarity with regulatory and permitting processes for fisheries engineering projects is a plus. Our mission is to help balance engineering, regulatory, and science based technical expertise with practical experience to solve our client's challenging renewable energy, water, and natural environment projects.
$90,000 - $120,000 a yearExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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In-depth experience of QC analytical methods and regulatory/pharmacopeia requirements for biologic or cell/gene therapy product testing and method validation for US, EMA and ICH regulations and guidance documents.
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Expertise in purification technology and process development, transfer to cGMP manufacturing plants, and authoring CMC sections of regulatory filings. For inquiries, mailto:sarah.lomas@evotec.com) Senior Talent Acquisition Specialist.
$135,000 - $185,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago
regulatory affairs jobs Title: regulatory affairs specialist Company: Jazz Pharma in Redmond, WA
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