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The Sr Clinical Trial Manager is accountable for delivery of selected and/or regional activities within a trial (e.g., manage and oversee vendor deliverables, collaborate with functions to set up activities (e.g. DM, IRT, eRT), support site activation and recruitment, support data review/cleaning activities, support PI/ICF development.
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The courses, learning activities, and resources provided to you in our pharmacy technician training program are designed to give you foundational and advanced knowledge, skills, and on-the-job experiences you need to prepare to become a certified pharmacy technician.
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Perform basic mechanical tasks with close supervision and oversight for daily tasks or, as part of a crew for larger activities including hoisting and rigging, working with vacuum and water systems, basic tooling, maintenance and troubleshooting of Neutral Beam subsystems.
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This includes Complaint Handling, Adverse Event Reporting, Health Hazard Evaluations (HHEs), Field Actions, and Post Market Surveillance activities required for EU MDR and other global regulatory bodies.
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The individual will be responsible for TM and clinical biomarker activities to support drug development programs in multiple diseases in neurology and neuropsychiatry. Able to conceptualize broad impact of research programs and personal activities in terms of site.
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The Sr Calibration Technician will also support functional and operational improvements of instrumentation and controls used within the CMC and ensure that all activities are completed safely within OSHA and internal standards.
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Raytheon has an exciting opportunity for an Associate Director, Global Trade who will oversee and manage the export/import licensing team and all export compliance activities within Raytheon's Advanced Products & Solutions (APS), Space, Imaging and Microelectronics (SIM) business.
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This includes overseeing the daily global eTMF system related activities relating to clinical study Trial Master Files (TMF), ensuring regulatory inspection-readiness and compliance with applicable laws and regulations.
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Support client facing activities for the cell therapy process development team. The ideal candidate for this position should have work experience in cell therapy process development, manufacturing science, analytical development, and familiarity with GMP/FDA/ICH guidelines.
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Actively looking for a Senior Scientist, Cell Therapy Process Development contributing to the development of early and late stage clinical cell therapy manufacturing processes. Experience with common equipment used in cell therapy manufacturing such as Sepax, Lovo, G-Rex, Xuri Bioreactors, CliniMACs Plus, CliniMACS Prodigy, MaxCyte GT.
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Oversee the measurement and evaluation of Hematology & Cell Therapy Medical activities, ensuring alignment with organizational objectives and priorities. BA/BS degree required; Advanced degree preferred (e.g., MD, PhD, PharmD, MBA.
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The Assoc II, Warehouse Ops assists on Inbound or Outbound activities as requested by the Warehouse Supervisor meeting quality, safety, productivity and operational standards. Example equipment in the facility may include order picker (cherry picker), forklift, reach truck, turret truck, pallet jack, and walkie rider.
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The Senior Scientist, Cell Therapy Process Development is responsible for development and technology transfer of internal and client related projects. The cell therapy process development team at is actively looking for a Senior Scientist, Cell Therapy Process Development contributing to the development of early and late stage clinical cell therapy manufacturing processes.
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Associate Director, Medical Affairs Cell Therapy, Franchise Strategy And Operations, Project Manager
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Global Medical Affairs, Strategy and Operations is responsible for the global planning activities of the Hematology Medical Affairs Department, including global/regional brand and medical planning, budget planning, congress planning, workforce planning, and planning and execution of special projects.
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Execute cGMP manufacturing activities, including CIP/SIP, media prep, cell culture sampling, and harvest operations. Expertise in aseptic technique, CIP/SIP, and bioreactor operation. Execute cGMP manufacturing activities, including CIP/SIP, media prep, cell culture sampling, and harvest operations.
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activities job in Princeton, NJ
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