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Req ID : 1435 Working Title : Kidney Transplant Clinical Research Coord II Department : Research - Hepatology Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : EXEMPT Primary Shift : Day Shift Duration : 8 hour Base Pay : $58,864 - $100,068.
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The ideal candidate for this position will have significant experience in pre-clinical research endeavors, especially in the regulatory aspects of research conducted under IACUC and Safety Committee approvals, procedural training, and/or hands-on expertise in such research.
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Participate in Research and Grant Development by developing and participating in research in genetic counseling and medical genetics, develop institutional review board protocols, and participate in writing clinical research grants.
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One year of clinical experience as a board eligible genetic counselor or genetic counselor intern. One year of clinical experience as a board eligible genetic counselor or genetic counselor intern.
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The Clinical Research Coordinator II Non-RN (CRC II Non-RN) serves the AdventHealth Research Institute (AHRI) in the Rocky Mountain Region (RMR). + Certified Clinical Research Coordinator (CCRC) (per the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA.
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The incoming CAO will build upon an innovative and novel undergraduate medical education curriculum, propel graduate medical programs of excellence, grow inter-disciplinary educational and clinical research, and enhance faculty development programs while providing strategic leadership and oversight of Baystate's academic enterprise.
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The Development Officer III (Director of Development) for UofL Health – Brown Cancer Center (BCC) will play a pivotal role in cultivating, soliciting, and stewarding gifts for the BCC’s research and clinical trials programs and be responsible for developing and sustaining meaningful connections with donors, ensuring an unparalleled donor experience, and championing the overall advancement goals of the UofL Health - Brown Cancer Center.
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The Clinical Research Coordinator I (CRC) works within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DF/HCC Clinical Trials Office and/or Partners HealthCare Institutional Review Board (IRB.
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Prior experience with UCSF, particularly with research in the oncology setting, clinical trial billing, and institutional policies for study compliance and regulation. Clinical Research Coordinator (CRC) Supervisors / Protocol Project Manager.
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The Bioinformatics Subject Matter Expert will provide services in the Clinical and Basic Cancer Research Field, in Support of the NCI Center for Cancer Genomics. Support the continued growth of the GDC, CCG Office of the Director requires bioinformatics Subject Matter Expert service in the clinical and basic cancer research field with specific expertise, as well as knowledge of the GDC.
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Coordinate the activation and maintenance of clinical protocols, including review and completion of submissions, amendments, and adverse event reports as required by the UIC Institutional Review Board (IRB), Protocol Review Committee and grant sponsors.
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In addition, together with the Center for Global Health and Diseases (CGHD) in the department, the Department of Pathology support research from basic immunology to international clinical trials and NIH training grants in global health/infectious diseases.
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Ensures that all activities are completed by strictly following Good Clinical Practices (GCP) & all relevant current local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal Regulations (CFR), & the International Conference on Harmonization (ICH.
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Our studies combine techniques from behavioral science, machine learning, and implementation research and incorporate influences from other fields including economics, health policy, biostatistics, epidemiology and clinical medicine.
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It has research, clinical and teaching relationships with the VA Long Beach Healthcare System and Childrens Hospital of Orange County (CHOC). Ability to work effectively with a wide range of management & medical staff, as well as representatives of regulatory agencies & businesses Knowledge and experience in planning and implementing clinical outpatient and clinical research facilities in compliance with Titles 22 and 24 of the Uniform Building Codes.
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