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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 Yesterday - 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 7 days ago - UpvoteDownvoteShare Job
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This position works with the National Director of State Legislative Affairs and other departments within T-Mobile to prioritize among various issues of importance and to ensure uniformity in the delivery of corporate policy positions.
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Just-Evotec Biologics is seeking a Director/Sr. Director of Regulatory CMC to join a fast-paced, collaborative and multi-disciplinary team to lead all aspects of regulatory affairs for the advancement of low-cost biotherapeutics manufacturing.
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Senior Regulatory Affairs Manager (U.S. Hub based location) The Senior Regulatory Affairs Manager will develop and communicate a vision for the RA function to management, including the development of global regulatory strategy in the area of regulatory submissions.
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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.
$100,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Create and own documentation of cellular core network design, integration and performance metrics for international expansion strategy for direct to handset such as IMS and EPC products, 3GPP feature and interface support, regulatory.
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Extensive management experience in a cGMP testing laboratory environment, with knowledge of regulatory and compendial guidelines as related to cell-based assay requirements, aseptic processing, and biosafety of cell therapy products.
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Work with the Safety, Regulatory, Operations, Manufacturing, Supply Chain, Quality teams as well as outside partners to ensure smooth product launches. - Experience designing systems that meet stringent compliance and regulatory standards.
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Execute necropsy/histology techniques directed by study protocols (regulatory, exploratory and investigative). Perform all assigned routine necropsy and histology tasks in a timely manner and in agreement with the SOP and guidelines in place, from necropsy room preparation to archival of specimens.
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Have a minimum of 8 years' experience with NEPA assessments and federal, state, and local regulatory compliance/permitting in the U.S. Advanced degrees may be used to fulfil part of this experience requirement.
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The Disability Resource Center reports to the Dean of Student Support in the Student Affairs division. Position Summary The Accommodations Assistant position works closely with the Alternative Formats Access Specialist and the Front Desk Program Assistant to assist with the reader/scribe accommodation, the alternative formats accommodation and the furniture accommodation.
$39,624 - $52,596 a yearPart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The ideal candidate is an experienced trust & safety professional who can translate work across compliance and Integrity teams seamlessly and act as the human API between GRC, Legal, Regulatory Offices, and the business, maintaining deep Integrity subject matter expertise.
$118,000 - $172,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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This investigation includes but is not limited to a criminal, civil litigations and regulatory review, employment, education, and credit review (role dependent). Series 07 - FINRA, Series 63 - FINRA, Series 65 - FINRA, Series 66 - FINRA.
$115,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Alongside Sales and Process Engineering, you are responsible for developing water treatment solutions for clients under complex technical or regulatory requirements. We design, supply, and service a range of water systems and monitoring equipment in industries ranging from pharmaceutical to food and beverage applications, and from microelectronics ultrapure water to municipal water and industrial wastewater treatment.
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regulatory affairs jobs Title: regulatory affairs specialist Company: Jobget in Redmond, WA
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