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About the Company At AMN Healthcare, we strive to be recognized as the most trusted, innovative, and influential force in helping healthcare organizations provide quality patient care that continually evolves to make healthcare more human, more effective, and more achievable.
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Forward is on a bold mission to make high quality healthcare available to a billion people across the globe. We are looking for a motivated Medical Assistant who thrives in a collaborative, innovative tech environment.
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Establish and maintain rigorous quality control and quality assurance processes. The Director of NGS will oversee the next-generation sequencing workflow across the clinical and R&D teams, ensuring the highest standards of quality, efficiency, and innovation.
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Product Oversight : Ensure exceptional execution in delivering top-tier Software-as-a-Service (SaaS) solutions, maintaining a keen eye on product quality and user-centric design. With a focus on scientific computing and GPU acceleration, this role is pivotal in ensuring the efficient performance and scalability of our high-speed computing technology to deliver high-quality SaaS solutions.
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Inform Quality Assurance team on any quality deviation of sample management and clinical sample testing. Oversee the trial master file (TMF) documents owned by VBD in accordance with regulatory requirements and the Takeda Quality management system.
$170,500 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Coordinate contract and budget negotiations between sites and internal function team and coordinate investigational product release authorization with quality assurance. The Clinical Trial Manager, Site Start-up will lead internal process improvements related to study start up activities to ensure clinical trials are executed with high quality standards in compliance with regulatory requirements, GCP, and company SOPs.
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The Senior Director of R&D Quality Assurance is responsible for establishing and implementing the strategy for the R&D QA function that provides Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), and Good Laboratory Practices (GLP) quality oversight at Apellis.
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Job Description & Requirements Specialty: MRI Technologist Discipline: Allied Health Professional Start Date: 09/30/2024 Duration: 13 weeks 36 hours per week Shift: 12 hours Employment Type: Travel MedPro Healthcare Staffing , a Joint Commission-certified staffing agency, is seeking a quality MRI Tech for a contract with one of our top healthcare clients.
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The role of Manager, Clinical Quality Assurance, supports Quality oversight for Bicycle’s development programs, ensuring compliance with applicable GLP and GCP standards and global regulations.
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Strong hands-on quant research, data and infrastructure skills including model management and data quality. We assist companies and non-profit organizations in delivering benefits to their employees.
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Experience writing change controls for biotech (biologics preferred) in an electronic Quality Management System such as Veeva or Trackwise. Arcadis DPS Group is a global EPCM firm offering full-service solutions within the Life Sciences (pharmaceutical, biotechnology, and medical technology) and Advanced Technology (semiconductor, data center, and solar) industries.
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Interfaces regularly with the Director, Research Compliance/Assurance & Programs to ensure compliance with all regulations Major Programs Management Manage Pre and Post award administration for assigned center-wide grants and federal contracts, by serving as the front-line guide and support for faculty and staff.
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Reporting to the Provost, the Assistant Vice President for Institutional Effectiveness is tasked with maintaining and refining institutional assessment and effectiveness processes to enhance the quality of educational programs, improve student outcomes, and ensure compliance with federal and state regulations.
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Reporting to the Senior Director, Analytical Development & Quality Control (QC), the Associate Director of Quality Control will be acting as QC lead, responsible for leading and managing the QC activities of PepGen’s pipeline.
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Experience with pharmaceutical data sources (e.g., IQVIA or Symphony claims, specialty pharmacy data, and Syndicated data sources); Deep understanding across various pharmaceutical data facets/processes, including data creation and acquisition, management, governance, data quality, integration, visualization and statistical modelling.
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quality assurance jobs Title: quality assurance assistant in Boston, MA
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