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The Clinical Research Coordinator assists the clinical trials process by registering hematology, oncology, and bone marrow transplant patients for clinical studies, assessing eligibility criteria, maintaining current protocol packets and assuring that all quality assurance measures are maintained within the protocol/study.
$39,300 - $64,349 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Manages and coordinates all facets of assigned clinical protocols from IRB preparation through query and data seal; ensuring protocol and regulatory compliance. The Ivy Brain Tumor Center is a non-conventional, non-profit program offering state-of-the-art clinical trials for patients with the most aggressive form of brain cancer.
$30.55 - $44.3 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Relevant certification as a Certified Clinical Research Professionals (CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB Professional (CIP) upon hire or within six months of hire.
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As a Junior Clinical Research Coordinator, you are responsible for assisting with the management and coordination of all aspects of conducting clinical trials within s RII, surgery centers, both clinically and administrative/regulatory.
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The range of these research projects are extensive and comprehensive, extending from biomarker/natural history studies to Investigator Initiated studies to Industry clinical trials (Phases 1-3.
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Using a disease-specific centers model for conducting clinical trials, CRS provides study development and implementation assistance, submissions to the FDA, IRB processing, patient recruitment, study coordination, study-specific training, data collection, and specimen collection and processing.
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Manages and coordinates all aspects of conducting clinical trials within Sentara Healthcare, both clinically and administratively. Manages and coordinates all aspects of conducting clinical trials within Sentara Health both clinically and administratively.
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Posted Job TitleClinical Research Coordinator A/B (Palliative Research Center)Job Profile TitleClinical Research Coordinator AJob Description SummaryThe Palliative and Advanced Illness Research Center is seeking a full-time clinical research coordinator who will be responsible for supporting multiple components of a mixed-methods study that aims to design a novel outcome measure for future trials of patients with acute respiratory failure (ARF.
$37,220 - $65,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Under the supervision of the Clinical Research Program Manager, the Clinical Research RN ensures the integrity and quality of clinical trials are conducted and maintained in accordance with federal, state, and local regulations, Institutional Review Board ("IRB") approvals, and Healthcare System policies and procedures.
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Under the supervision of the Clinical Research Program Manager, the Clinical Research RN ensures theintegrity and quality of clinical trials are conducted and maintained in accordance with federal, state, andlocal regulations, Institutional Review Board ( IRB ) approvals, and Salinas Valley Memorial HealthcareSystem ( SVMHS ) policies and procedures.
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Supports IRB approved clinical research/trials though a variety of activities including but not limited to: obtaining consent; ordering diagnostic tests; recording laboratory and diagnostic results; administering therapeutic interventions; and documenting and reporting patient outcomes including toxicities or adverse events.
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Demonstrated ability to gain understanding of the federal and institutional regulations and policies governing clinical research involving protection of human subjects (JCAHO, FDA, GCP, OHRP, IRB NIH/NCRR for PCRC only.
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May compile information necessary for continuing review by local IRB or for Network Principal Investigator annual continuing review for USOR trials. Under general supervision is responsible for supporting the regulatory team with coordinating the research regulatory and administrative activities of clinical trials for the practice.
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The Program Coordinator may assist the Principal Investigator with IRB-related issues as well as helping to prepare new grants / clinical trials. Assist with the preparation of annual reports and IRB communications.
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The Institute oversees 600,000 sq ft of dedicated space and the administrative and operational infrastructure for basic and applied research and clinical trials, including more than 20 advanced tech core facilities, extramural funding management, regulatory and legal strategy and compliance, and product development and commercialization.
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