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Manages submission of regulatory documents in accordance with IRB, federal, industry, and institutional guidelines and requirements. IRB submission experience preferred. Position Summary: The Clinical Research Coordinator III, as a certified research professional, handles clinical trial administration for all protocol phases for the Leukemia and Lymphoma Disease department.
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Attending required faculty training (e.g., Canvas, IRB, HR) and departmental, college, and university meetings. Under the direction of the Applied Psychophysiology Department Chair, the Adjunct Faculty Member is responsible for modeling instructional excellence in teaching and mentoring activities.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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In this role, you will be responsible for preparation, submission and maintenance of regulatory applications to fulfill research requirements for open studies in addition to working with Sponsor monitors to timely process, review and collect regulatory documents maintained in the Investigator Site File. All work should be completed according to good clinical practice (GCP), JCCC CRU standard operating policies (SOP), UCLA Institutional Review Board (IRB) and government regulations.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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IRB Administrator University of California Los Angeles Requisition Number: 33600 Salary: $5,167 - $13,233 monthly Position Description: The Office of the Human Research Protection Program (OHRPP) is a part of the Office of Research Administration (ORA) and supports the $1 Billion annual research program at UCLA by providing leadership, professional guidance and administrative services to faculty, department administrators, and students.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Your responsibilities will extend to the development and refinement of project materials and protocols, active participation in crafting comprehensive project reports, and the meticulous creation, review, and management of Institutional Review Board (IRB) applications and records.
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Assists in writing of grant applications, IRB applications, publications, white papers, standards, SOPs and presentations. The Clinical Research Informatics (CRI) is a core group at SC CTSI that provides expertise and support for clinical research data integration, data sharing and data security to help drive the integration of clinical care and clinical research.
$175,000 - $220,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Act as the physician leader on the Institutional Review Board (IRB) Committee and development of sustainable IRB process in support of resident and faculty research opportunities. Assist the Program Director and Program Coordinator, in collaboration with the Residency Program Coordinator, the BHRS Medical Director, BHRS Deputy Medical Director, Designated Institutional Official, in support of the psychiatry residency program.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Min 2 yrs exp in a clinical research coordinator role, College Degree, exp with IRB procedures, recruiting and enrolment, completing CRFs. Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, etc.
$30 - $35 an hourExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Responsible for overseeing daily business office transactions, coordinating academic affairs searches, managing Dean's Office events, providing Institutional Review Board (IRB) support, offering committee support, and maintaining the websites for Academic Affairs and the Dean's Office.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Assists researchers in genetic program evaluation and genetic research evaluation, as well as grant writing and interaction with the Institutional Review Board (IRB). Assists researchers in genetic program evaluation and genetic research evaluation, as well as grant writing and interaction with the Institutional Review Board (IRB.
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As a Genetic Counselor by the American Board of Genetic Counseling. In addition to its direct clinical services, DHS also runs the Emergency Medical Services (EMS) Agency and the County's 911 emergency response system, as well as Housing for Health and the Office of Diversion and Re-entry, each with a critical role in connecting vulnerable populations, including those released from correctional and institutional settings to supportive housing.
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Serves as contact for subjects, study personnel, Institutional Review Board (IRB) and study sponsor. Ensures consent process is performed and documented in compliance with FDA, GCP, IRB, HIPAA, SOPs, sponsor and institutional regulations and policies.
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Prepares and maintains case researchers in genetic program evaluation and genetic research evaluation, as well as grant writing and interaction with the Institutional Review Board (IRB). Prepares and maintains case researchers in genetic program evaluation and genetic research evaluation, as well as grant writing and interaction with the Institutional Review Board (IRB.
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Reporting to the provost and vice president for academic affairs, the associate vice president for research supervises the Office of Research, Scholarship, and Creative Activities (ORSCA), serves as the institutional officer for the Institutional Review Board-Human Subjects (IRB) and the Institution Animal Care and Use Committee (IACUC), and collaborates closely with the Office of Sponsored Projects in University Auxiliary Services (UAS), the University Foundation, and University Advancement.
$175,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago
irb job in Los Angeles, CA
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