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The Research Nurse manages and coordinates all aspects of conducting clinical trials, both clinically and administrative/regulatory. Screens, consents, enrolls and follows study subjects and oversees the same by non-RN clinical research coordinators, ensuring protocol compliance and close monitoring while subjects are on study.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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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 comprehensive network encompasses six acute-care hospitals, an extensive medical group with primary, specialty and urgent care services, a cancer care network, outpatient surgery centers, clinical research, medical education, a foundation, an accountable care organization, community services and more.
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SUMMARY - Manages and coordinates all facets of assigned clinical protocols from IRB preparation through query and data seal; ensuring protocol and regulatory compliance. One year RN experience within clinical research.
$30.55 - $44.3 an hourFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Reviews studies for clinical and operational feasibility, along with the Investigator and Director of Research. Clinical Oncology and/or prior research experience required.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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You must be adept at cultivating strong collaborative relationships across Medical & Scientific Affairs as well as Infection Prevention & Control, Quality Affairs & Regulatory Affairs, Research & Development, Legal, and Health Care Compliance.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Clinical Research Coordinator Apply! This position provides administrative / regulatory support (recruiting, interviewing and scheduling study participants, processing IRB and other regulatory documents) to specific clinical departments in accordance with all federal, state, regulatory agency, and specific institutional requirements.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Proclinical Staffing is seeking a Senior Director, Regulatory Affairs to join a leading health information technology and clinical research organization. Typically requires 15-20+ years relevant clinical research and/or regulatory experience with multi-regional and global focus including significant experience in senior strategic role, including specific oncology investigational product experience.
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This position, under the direction of the Senior Director, Revenue Integrity, is responsible for acute and ambulatory clinical, coding and regulatory research. Routinely performs regulatory research and provides guidance to the revenue cycle partners on regulatory changes, or in response to requests for interpretive guidance on billing or regulatory concerns.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Reviews and responds to all regulatory requirements for all study protocols; assists with all required forms/documents for initial study with IRB. Schedules medical procedures/tests necessary for research, including blood draws and imaging studies.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Celerion is committed to swift, exceptional clinical research through translational medicine. Manage the complete sample management aspect of all assigned studies by working a flexible schedule (including additional hours when needed), cross-checking the work of teammates and proactively communicating with the Clinical Conduct Manager, Clinical Study Manager, Clinical Sample Handling Specialist Team Leader, sponsor contact or receiving laboratory as appropriate.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Regulatory compliance is crucial due to integration of sponsored clinical studies. Investigating initiated trials, Grant submission, Regulatory Compliance (5+ years) Collaborate within the organization on regulatory standards.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The ideal candidate has previous experience in clinical research coordination, with a strong attention to detail and a passion for contributing to medical advancements. Provide oversight and quality control of our internal regulatory filing system.
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Ensures assigned studies are conducted in accordance with the Food and Drug Administration (FDA), Office for Human Research Protections (OHRP), Good Clinical Practices (GCP), Institutional Review Board (IRB), HIPAA regulations and institutional requirements, which includes, but not limited to, the following duties: Knowledge of all regulatory requirements and institutional requirements when conducting the study protocol(s.
$30.55 - $44.3 an hourExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
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clinical research regulatory jobs in Phoenix, AZ
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