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A veteran of the U.S. military, ground, naval or air service who is entitled to compensation (or who but for the receipt of military retired pay would be entitled to compensation) under laws administered by the Secretary of Veterans Affairs; or.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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As part of the MMS US Region Integrated Communications team, you will partner with Marketing, Medical Affairs, Regulatory, and Legal to streamline the advertising and promotional (AdProm) content and claims review process, working closely with the marketing team as well as key members of the sales team and other cross-functional partners involved in messaging, claims, content development, and sales training.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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International Regulatory Affairs Specialist (LATAM) 5+ years of medical device experience with BS degree and work experience in Regulatory Affairs, or 3+ years of medical device experience with MS degree and work experience in Regulatory Affairs, or 2+ years of Regulatory Affairs experience with PhD in Engineering/Science.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Reporting to the Vice President of the Diagnostics and Genomics (DGG) Quality organization within Global Quality and Regulatory Affairs (GQRA), the Director of Clinical and Safety Quality Assurance will be responsible for setting strategy for and leading the Clinical and Safety Quality Assurance function for Agilent.
$240,581 a yearFull-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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In addition to your research training at LJI, UCSD Office of Postdoctoral and Research Scholar Affairs offers professional development and career training opportunities to ensure you achieve the highest level of academic and research excellence.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Primary responsibilities are to support Shell Energy's wholesale/retail trading/origination businesses and Shell Renewable and Energy Solutions related businesses through external advocacy for competitive markets, communicating regulatory changes and impacts of regulatory changes to commercial teams, conducting due diligence on deals to facilitate commercial transactions within existing regulations and managing compliance obligations.
$218,000 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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VETS is a Department of Veterans Affairs, Center for Veterans Enterprise (CVE) certified Service-Disabled Veteran-Owned Small Business (SDVOSB). Based in Tysons Corner, Virginia, VETS has a Southwest operations office in Sierra Vista, Arizona and contract management sites throughout the United States.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Targeting 5+ years of prior MI and MLR experience in pharmaceutical or biotech industry or relevant experience in medical affairs, medical communications, scientific affairs or similar area.
$182,400 a yearFull-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Clinical Affairs/Novel Biomarker Discovery: Focus on early feasibility and novel biomarker discovery. Assay Development: Focus on feasibility, verification and validation of new assays for commercialization.
$27 an hourFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Primary responsibilities are to support Shell Energy's wholesale/retail trading/origination businesses and Shell Renewable and Energy Solutions related businesses through external advocacy for competitive markets, communicating regulatory changes and impacts of regulatory changes to commercial teams, conducting due diligence on deals to facilitate commercial transactions within existing regulations and managing compliance obligations.
$218,000 a yearExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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This position is part of the Quality Assurance and Regulatory Affairs group located in Coralville, IA, USA and will be remote. Support a team responsible for worldwide submission activities, maintenance of approvals and global regulatory strategies, across multiple sites, in support of PMA, 510(k), de novo, technical files, pre-submissions, annual renewals, change notifications, post-market surveillance activities, etc.
$100,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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The Medical Support Specialist follows guidance provided by BioLife Medical Affairs and provides center level support of environmental, health and safety (EHS). + You can be a Pandemic Coordinator when authorized by EHS and support investigations associated with pandemic threats within the local community as indicated by EHS or Medical Affairs.
$50.24 an hourExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Bachelor’s degree in Communications, Public Affairs, English, Public Relations, Marketing, Journalism, Public Administration or similar required. 4+ years previous Public Relations, Public Affairs or Community Relations experience required.
$80,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Collaborate cross-functionally with internal stakeholders including MSL field directors, medical communications and information, clinical development, medical affairs, HEOR, and pharmacovigilance to identify and develop content and training material for ACADIA disease state and investigational or approved product trainings.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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We are looking for an experienced and detail-oriented Regulatory Affairs Specialist to ensure compliance with global regulatory standards and facilitate successful product approvals. Job Title: Regulatory Affairs Specialist.
Full-timeExpandApply NowActive JobUpdated 24 days ago
affairs job in San Diego, CA
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