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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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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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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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Review/approve creation/modifications to Master Stability Protocols (MSP) and Study-Specific Protocols (SSP), batch-specific enrollment documentation, and LIMS stability studies. Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you.
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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, clinical trials, cancer chemoprevention, basic and clinical pharmacology, novel cell therapy constructs, and participation in a broad range of teaching initiatives.
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Utilize your extensive master data expertise to demonstrate a profound understanding of SAP MDG Materials, BOM, Recipes, MRP, MPS, Work Centers, Batch Management, Quality Inspection, Costing among others.
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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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The Stability Senior Scientist reports to the Senior Principal Scientist or Associate Director of GBS and is responsible for end-to-end oversight of product stability programs. Use computer software/programs: Microsoft Office applications, SAP, LIMS, Quality Management System (e.g. TrackWise or Veeva), JMP, etc.
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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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Use computer software/programs: Microsoft Office applications, SAP, LIMS, Quality Management System ( TrackWise or Veeva), JMP, etc. A thorough knowledge of cGMP regulations as referenced in The Code of Federal Regulations (CFR) and their specific application to stability programs in a pharmaceutical manufacturing facility.
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The Engineer I, CAR-T Clinical Manufacturing Sciences & Technology is responsible for supporting the production of personalized cell therapy products for global clinical trials. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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The PA will serve as a back-up and clinical resource for the neurosurgical/pain management ambulatory care nurse(s) assigned to outpatient phone calls and management of outpatient clinical issues including but not limited to reviewing imaging, laboratory and neurophysiological test results.
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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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Minimum1 year of clinical experience in OB/GYN ultrasound. 5 years of clinical experience in OB/GYN ultrasound. Minimum1 year of clinical experience in OB/GYN ultrasound. 5 years of clinical experience in OB/GYN ultrasound.
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clinical master file jobs Title: trial master file in Piscataway, NJ
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