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The Senior Research Associate position will function as a quality-control and radiochemistry specialist , which is essential to the quality delivery of investigational radiopharmaceuticals for clinical practice and research at UT Southwestern in full compliance with FDA's regulations.
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The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
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Minimum Qualifications Minimum Education: High School Diploma or Equivalent Minimum Years of Experience: 4 Years of clinical or hospital experience; 2 Years of experience in quality or utilization review.
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Clinical Nurse Specialists assess, plan, provide and evaluate specialized nursing care of patients by advancing the quality and scope of nursing practice through clinical practice, education, research, consultation, and administrative roles in the area of clinical expertise (e.g., diabetes, cardiology, respiratory, pediatrics, etc.
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Clinical Quality Specialist Benefits At TidalHealth, team members working at least 36 hours per pay period based on 12-hour shift schedules or at least 37.5 hours for non 12-hour shift schedules and part-time team members working at least 30 hours or more on weekends only are eligible for benefits.
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PROGRAM DESCRIPTION The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
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Position Focus: Reporting to the YCCI Quality Assurance Audit Manager, the incumbent conducts clinical research auditing and quality improvement efforts for human subject research conducted at the Yale Medical School.
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Bachelor's Degree in medical research, scientific, health care related, or regulatory discipline, 3 years’ experience in IRB operations or in the conduct and/or monitoring of research in a clinical or regulatory environment.
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As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products.
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Assist in dissemination of clinical staff to improve the quality of care based on the dissemination of the results. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and cancer treatment centers and outpatient facilities in the Atlanta, Chicago and Phoenix areas.
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The Quality System Specialist will play a role in supporting the Northern California quality management Customer Request request Process for Life Science (LSG) and Clinical Diagnostics (CDG) products.
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The incumbent is tasked with supporting and conducting high-quality translational and clinical research to facilitate the development of infectious disease countermeasures for US military personnel.
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The incumbent participates in the implementation and maintenance of the quality management system (QMS), with a focus on one or more program areas, including collection of blood and cellular therapy products, manufacturing and distribution, clinical services, transfusion services, laboratory services, and clinical research, as well as organization-wide support functions such as information systems, facilities, and safety.
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Clinical Research Regulatory Specialist B. Regulatory Affairs as a field is concerned with ensuring that clinical research is conducted in a safe and legally compliant manner.
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35% Quality Assurance Education Specialist: In tandem with the QAE Program Manager participates in onboarding and training CTO staff on Standard Operating Procedures (SOPs), MUSC IRB policies, Good Laboratory Practices (GLPs), Good Clinical Practices (GCPs), and ICH Guidelines.
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clinical research jobs Title: quality specialist in Marion, Indiana
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