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Quality Control Inspector - Second ShiftDevens, MAEngineering – Quality /Full-time /On-siteCommonwealth Fusion Systems (CFS) has the fastest, lowest cost path to commercial fusion energy. CFS collaborates with MIT to leverage decades of research combined with groundbreaking new high-temperature superconducting (HTS) magnet technology.
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The department provides a strong infrastructure that enables researchers to successfully compete for external funding and pursue scholarly activities, including robust pre- and post-award administrative support, a Data Management and Analytics Core with several PhD-level biostatisticians, analysts, and data managers, and a well-trained pool of clinical research staff.
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Education, Knowledge, Skills and Abilities Preferred: National Certification in area of specialty preferred when eligibleLicenses and Certifications Required: NJ State Professional Registered Nurse License BLS/CPR certification by American Heart Association is required within 60 days of hireLicenses and Certifications Preferred: Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC.
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As a Clinical Laboratory Scientist III, you will be responsible for: performing complex medical laboratory tests for diagnosis and treatment of disease, analyzing and assuming accountability for accurate test results, maintenance of complicated instruments, monitoring quality control and quality assurance programs, assuring compliance with regulations and standards of regulatory agencies, and managing special projects.
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Bachelor’s degree in biological sciences, health care management, or life sciences research; BSN/RN or experience in clinical trial management. Proficiency in Microsoft Office (Word, Excel, Outlook), Smartsheet, electronic TMF, and other electronic clinical technologies.
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The principal duty of the control operator (CO) is to acquire the knowledge, skills and experience necessary to qualify to perform Licensed Operator duties and successfully pass the NRC's Reactor Operator's License examination.
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The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs. Key Responsibilities In collaboration with other members of the clinical research site team works to ensure the execution of assigned studies.
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We encourage applicants from all areas of interest, including but not limited to Control Systems, Robotics, Electronic Warfare, Electromagnetics and Antennas, Embedded Systems, Computer Systems, Machine Learning, Microelectronics, VLSI, IC Design, Communication and Networks, or any other closely related field.
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A minimum of 3-5 years in Analytical Development and/or Quality Control preferably in a clinical stage biopharmaceutical company. Scientist, Analytical Development & Quality Control Dyne Therapeutics is a clinical-stage muscle disease company focused on advancing innovative life-transforming therapeutics for people living with genetically driven diseases.
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The focus would be on maturing early-stage technologies for disruptive HVAC&R systems, which include breakthrough technologies in the areas of efficient sustainable non-vapor compression-based thermal solutions, IAQ control etc.
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5+ years of hands-on configuration experience with at least one of the following control systems: DCS (Honeywell, DeltaV, Foxboro), SIS (Triconex, DeltaV, Honeywell). Control Systems Specialist (DeltaV.
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We recognize that high-impact research programs can take many forms, including those that have potential for sustained extramural funding, drive paradigm changes in public policy and/or discourse, and/or pioneer the study of new and important areas within clinical psychology.
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The incumbent will function as a Psychometrist in the interdisciplinary clinical research program on Alzheimer's disease, related dementias, and healthy aging, under the general supervision of licensed Clinical Psychologists specializing in Neuropsychology.
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Embedded within Tempus as on onsite researcher, the postdoctoral fellow will have direct access to over 150k de-identified samples with genomic and clinical data, a large organoid repository with genomic and pharmacological screening data, a huge computational environment, and mentorship and collaboration from clinicians, molecular biologists, and data scientists.
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Resources include dedicated 3D technologists for advanced fMRI/DTI, MR guided High intensity frequency ultrasound, intraOp 3T, 4 research-dedicated scanners (PET-CT, two 3T MR, PET-MR), cyclotron, and GMP radiopharmaceutical production facility, full spectrum of small animal imaging equipment, clinical research administrative team.
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clinical research control jobs Company: Ucla Health in TX, Us
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