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Experience in Labware Modules like LIMS Stability, EM, Inventory, Storage Location Management, Instrument Interfaces, Lot, Sample Management for Clinical Trial & Manufacturing Domain. Experience in Labware Modules like LIMS Stability, EM, Inventory, Storage Location Management, Instrument Interfaces, Lot, Sample Management for Clinical Trial & Manufacturing Domainhas context menuCompose.
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A PhD in oncology/immuno-oncology, or related field, with at least eight (8) or more years of translational research, applicable biomarker, and/or clinical trial experience. A strong publication record demonstrating relevant experience in drug development, translational research, biomarkers and/or clinical trials.
$142,500 - $237,500 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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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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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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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Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential.
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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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Court Interpreter 2- Master - The salary range for this position is $73,674.60 to $111,206.94 for Schedule A, and $73,674.60 to $105,646.59 for Schedule B. Employees at this level may interpret complex legal proceedings; translate forms, letters and other court-related documents; mentor Court Interpreters; and interpret for trials that are high profile, complex, and which involving crimes of the first degree.
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Familiarity and experience in establishing clinical biomarker analyses for clinical trials. Overview Within the Translational Bioanalytical Sciences (TBS) group of Clinical Development, the role focuses on LC-MS/MS of small and large molecule quantitative assay development of biological samples.
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Clinical Nuclear Medicine Technologist background with a minimum of 3 years MI SPECT clinical experience required. Our portfolio of products, services, and solutions is at the center of clinical decision-making and treatment pathways.
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Report directly to the Administrator, Executive Director or Patient Care Manager Senior and function under the direction, instruction and supervision of the Registered Nurse and/or Clinical Supervisor.
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The Mr. Appliance Academy is designed to take you from Apprentice to Master Technician quickly. If you enjoy taking care of the customer, are awesome at troubleshooting, and love working with your hands and technology, a career at Mr. Appliance as an Appliance Repair Technician could be your future.
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Assist in review and release clinical trial supply (investigational product) for use in human clinical trials; issuance of Certificate of Analysis/Conformance. Serve as the GLP/GCP subject matter expert to cross-functional clinical trial teams to ensure that all quality and regulatory compliance activities were conducted in compliance with GCPs, SOPs and ICH Guidelines.
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Own the end-to-end architecture of the modern Safety/Pharmacovigilance Data Platforms which ingests data from the several systems across clinical, non-clinical systems and transforms it into insights for internal and external users using a scalable big data pipeline on GCP.
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And other clinical trial activities for solid tumor, high enrollment, adult population Oncology related trials. Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions.
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clinical trials trial master file jobs Title: trial master file in Somerset, NJ
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