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The Director/Sr Regulatory Affairs will lead the overall CMC Regulatory strategy for Adverum’s gene therapy program/s. Manage the Regulatory Affairs (CMC) Strategy for Regulatory Affairs.
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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.
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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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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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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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Our customer, a software company , is looking for a Regulatory Counsel who will work on the exciting legal issues surrounding transformational autonomous driving technology and help drive business lines forward from technology ideation through scaled commercial deployment.
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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. Senior Regulatory Affairs Specialist I.
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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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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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Meet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs professional to join their team. This position will be reporting into the SVP of Regulatory Affairs and will be supporting Clinical Regulatory and Regulatory CMC functions.
$240,000 - $280,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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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. Write and edit clinical and scientific reports for regulatory submission and scientific communication.
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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.
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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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Our Client, the pioneer of and global technology leader in robotic-assisted surgery has a Regulatory Post Market Surveillance opening in Sunnyvale, CA. Escalating complaints to the Regulatory Post Market Surveillance Manager when new failure modes are encountered.
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affairs job Title: regulatory affairs Company: Thermo Fisher Scientific in Stanford, CA
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