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Stanford University seeks an accomplished leader to serve as Director of Human Resources for Student Affairs. Human Resources Director for Student Affairs. Participate in setting divisional objectives and goals, and design performance appraisal process for Student Affairs.
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This position is part of Clinical Affairs team and will be hybrid to Sunnyvale, CA. The senior clinical research scientist will work on advanced, complex projects requiring state of the art knowledge in oncology and/or infectious disease molecular diagnostics.
$103,000 - $142,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Decedent Affairs Coordinator will interact with physicians, nursing staff, Pathology Department, police, medical examiner, risk management, security, etc. The Decedent Affairs Coordinator is responsible for coordinating the care of deceased patients after a demise within Stanford Health Care and Stanford Children's Health.
$39.28 - $51.07 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Support the work of the Korean office’s regulatory affairs (RA) team. We are seeking a highly motivated, full-time Regulatory and Quality Affairs Manager to join our growing company. ● Define quarterly goals for the Regulatory and Quality Affairs Team and give presentations on the team’s progress.
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This Senior Regulatory Affairs Specialist position is an on-site opportunity working out of our Santa Clara, CA location in the Abbott Vascular Division. 2-3 years of experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area.
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As a key member of Adicet's medical team, the head of Medical Affairs will be responsible for setting up and overseeing effective interactions with key opinion leaders, patient advocacy groups, and medical institutions in areas of hematology-oncology and autoimmune diseases relevant to Adicet's pipeline.
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The Vice President of Medical Affairs is responsible for providing clinical and scientific guidance in all areas of clinical risk, safety reviews, adverse experience reporting, product life cycle reviews, and protocol design.
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The Regulatory Affairs Senior Specialist I, NPD is responsible for evaluating and ensuring labeling accuracy for Cepheid’s in vitro diagnostic products. This role offers a unique opportunity to collaborate with cross-functional teams, including Technical Publications, Product Transfer, Quality, R&D, and Clinical Affairs, as part of Cepheid’s global change control process.
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Minimum of 7 years of experience in external affairs, advocacy, government relations, or related roles, preferably within the technology or financial services industry. Public Affairs: Represent &/or support others’ participation at events, conferences, and other forums to build relationships, foster awareness and trust in the platform and our team, and advance our programmatic and business goals.
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Minimum of 5 years of experience in CRMS/MA (e.g. medical science, clinical, affairs, regulatory affairs and/or healthcare economics) within the medical device or pharmaceutical industry with a Bachelor's degree, or 3 years with an advanced degree.
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Management of personal affairs, including travel arrangements, personal shopping, and lifestyle management. Management of personal affairs, including travel arrangements, personal shopping, and lifestyle management.
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Leverage internal and external resources to establish core domain expertise for medical affairs and clinical affairs initiatives. Vice President of Medical Affairs. At Varian, a Siemens Healthineers Company, we bring together the world's best talent to realize our vision of a world without fear of cancer.
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Administer and support Postdoctoral Affairs Program within the Department of Otolaryngology – Head & Neck Surgery. Administer and support Postdoctoral Affairs Program within the Department of Otolaryngology – Head & Neck Surgery.
$33.17 - $43.27 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As an onsite System Administrator on our project, you will be supporting the Department of Veterans' Affairs. MKS2 Technologies, LLC, an award-winning high growth small business, creates innovative and customer-centric technology solutions in the areas of Cyber Security, Instructional Design and Training, Software Engineering and IT Support Services to improve the security and well-being of our clients.
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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.
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affairs job Title: affairs Company: Thermo Fisher Scientific in Los Altos, CA
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