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Assists the clinical services team in the conduct and execution of clinical trials that include, but are not limited to: clinical planning, protocol development, essential document development, IRB submissions, CDAs and investigator agreements, and Trial Master File preparation and oversight.
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ENTA has a clinical alliance with The Mount Sinai Hospital for the treatment of diseases of the head and neck and esophageal cancer and a partnership with the American Cancer Society to educate and treat patients with smoking disorders and cancer.
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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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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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Develop & implement Master Data Management (MDM) strategies and ensure effective data governance exists to maintain accuracy and integrity of master data. Understanding of efficiency principles such as Lean/Six Sigma; Black belt preferred.
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In addition to providing clinical care, our academic institution in collaboration with Robert Wood Johnson Medical School creates unique opportunities for physicians to engage in clinical and research programs, faculty development, quality improvement activities, and participation in a broad range of teaching initiatives.
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A clinical liaison team available 24/7 to offer medical and professional support and career development. Triage Staffing is seeking a travel Cath Lab Technologist for a travel job in New Brunswick, New Jersey.
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The Vein to Vein team's patient-centric work is right in the middle of the action supporting both the Clinical & Commercial organizations early on from patient enrollment and order submission through to the treatment delivery and patient infusion.
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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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Collaborate with Protocol Activation office to initiate and activate all new clinical trial protocols assigned utilizing Oncore Study-start up task list. Vitalief, a fast-growing, “best of breed” Research and Clinical Trial Solutions Company, is committed to identifying talented and passionate clinical research professionals to join our exceptional team and support our clients in planning and executing successful clinical trials.
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Licensed Clinical or Counseling Psychologist in the State of New Jersey (required) We are seeking a Clinical Psychologist that is looking for a partnership in a growing organization with a strong team-mentality working in a juvenile facility, primarily with sex offenders.
$140,000 - $155,000 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Proven experience as a Data Architect or Data Modeler, specifically within the clinical or healthcare sector. Evaluate and interpret existing data structures to ensure optimal performance and alignment with industry standards in the clinical/healthcare domain.
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In terms of plasmid service, GenScript ProBio supports the most clinical approvals for CGT drugs including mRNA vaccines, CAR-T in China. GenScript ProBio’s total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.
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Lead, direct, coach, and develop an effective Operations team responsible for daily clinical and commercial production of autologous and allogeneic cell therapy products, while ensuring safe and compliant operations according to cGMP requirements.
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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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clinical trial master file jobs Title: trial master file in Somerset, NJ
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