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The New Jersey Judiciary consists of: the Supreme Court, the Superior Court including the Appellate Division and the Trial Court of the 15 vicinages in New Jersey, the Tax Court and the Municipal Court System.
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Job Title Master Tool Maker Days of week Monday - Friday Hours 7:00 am to 3:30 pm Location Piscataway, NJ Hourly Payrate $26/h - $30/h Type of role Temporary 3 to 6 months Safety shoes yes mask no Vaccination no other requirement Heavy Lifting other requirement none other requirement none.
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Experience with handling Prerogative Writ, Plenary Zoning, Affordable Housing litigation in trial and appellate courts, as well as land use applications before local Zoning and Planning Boards, County and State administrative boards and agencies.
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Your role will involve applying state-of-the-art AI techniques to extract valuable insights from various image modalities such as OCT (optical coherence tomography), FAF (fundus auto-fluorescence), and CFP (color fundus photography) in diseases such as dry AMD and IRDs. Through the use of these innovative technologies, you will improve our understanding of structural biomarkers during disease progression, ultimately enhancing clinical trial efficacy and efficiency.
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Develop a sequenced master production schedule (MPS) that outlines when and how much of each product should be manufactured to meet supply plan. By leveraging planning tools, continuous improvement methodologies, and cross-functional collaboration, the Director of Global Metals Planning & Master Production Scheduling plays a pivotal role in optimizing production workflows, reducing costs, and enhancing overall business performance.
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Englewood Hospital, a community teaching hospital founded in 1890, consistently earns high marks for clinical excellence and patient safety. Areas of clinical excellence offered by the health system include cardiac surgery and cardiac care, cancer care, orthopedic surgery, primary care, spine surgery, vascular surgery, and women’s health, as well as bloodless medicine and surgery and minimally invasive robotic surgery.
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Solid working knowledge of pharmacokinetics and modeling, PKPD principles, ADME concepts, and clinical pharmacology. The clinical pharmacologist will be responsible and accountable for designing clinical pharmacology programs and studies, performing PK and PKPD data analysis, supporting clinical dose selection and authoring summary and regulatory submission documents.
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This individual will support the organization in its build and ramp-up of clinical production and facility approval of a state of the art cell therapy facility. This position will be responsible for maintenance support and mechanical system operations for cGMP Clinical and Commercial Cell Therapy Manufacturing facility.
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Critical aspect of the role includes defining an agile quality and compliance strategy that supports Digital Data unit in their effort to establish a standardized, resilient, and sustainable data pipeline - including data sources, data quality, data governance, data management and master data management.
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Process Architecture, Process Design, Engineering, Construction, Commissioning, Qualification, LEAN Project Delivery, Strategic Master Planning, Energy Conservation Management, Project Controls, Program/Project Management, Operations/Logistics Strategy and Planning, EPCMV and Staffing Services.
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Set-up, organize, and maintain clinical study documentation (e.g. Trial Master File documents, clinical study site documents, email correspondence, training materials, etc.
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QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine.
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The DTS Business Process Owner will promote a manufacturing process excellence culture by identifying, developing and implementing program initiatives focused on manufacturing process improvement solutions within the highly integrated platform of SAP S/HANA, SAP-ME, & LIMS. The individual will lead and direct the activities of Process Experts, Super Users, Specialists and Trainers (where they exist) and directly manage DTS process experts and master data stewards.
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Receive clinical trial specimens according to laboratory protocols via LIMS or paper-based process. Legend Biotech USA, Inc. is seeking entry-level Scientists to join our Bioanalytical Sciences team responsible for daily Flow cytometry workflow to support immunophenotyping and cell-based assays of clinical samples.
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Our openings include receptionist, data entry, customer service, collections, office managers, call center, administrative assistant, accounts payable clerk, accounts receivable clerk, file clerk, warehouse, assembly, production, pickers, packers, forklift, machine operators, and maintenance mechanics.
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clinical trial master file jobs Title: trial master in Raritan, NJ
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