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A Clinical Research Coordinator I is asked to perform an increasing complexity of tasks to facilitate clinical trials at Virginia Mason, working with a variety of sponsors ranging from large pharma and biotech sponsors to small non-profit grant awards.
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The Clinical Research Manager (CRM) reports to, and is directly responsible to, the Assistant Director for the Clinical Trials Unit for all clinical research matters fulfilling the mission of the Chao Family Comprehensive Cancer Center (CFCCC), the University of California Irvine School of Medicine and the overall UC Irvine Health enterprise.
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Demonstrated knowledge of all components the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, patient care management, etc.
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Preferred: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) is preferred. Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification, along with a minimum of two years additional professional experience, will be considered in place of degree.
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Oversee the full life cycle of multicenter randomized clinical trials including study design and implementation; data collection tool development; data quality assessment and ongoing monitoring; regulatory reporting; statistical analysis; interpretation of results and manuscript writing for the Peripheral Artery Disease (PAD) research group.
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Under the direction of the Principal Investigator (PI) and Cardiology Research Nurse Manager, collaborate with all members of the clinical research team to ensure all federal, state, university, and protocol requirements are followed, institutional research objectives are met, and that ethical obligations are kept.
$55,000 - $75,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Reports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies.
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HHC is also an active member of the Alliance for Clinical Trials in Oncology and NRG Oncology and has access to clinical trials offered by these groups. The ideal candidate would work closely with the Director of Neuro-Oncology, Alexis Demopoulos, to develop and deliver advanced treatment options through clinical research while providing comprehensive, coordinated, and outstanding clinical care for patients suffering from primary and secondary central nervous system neoplasms as well as the neurologic complications of cancer.
$250Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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The Clinical Research Coordinator is responsible for coordinating and overseeing clinical operations of all assigned clinical trials and participates in assessing, planning, implementing and compliant study conduct according to all relevant local, federal, and state regulatory and institutional Polices and Standard Operating Procedures.
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Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up.
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Prepare all initial, amendment and continuing review submissions for assigned clinical trials, ensuring adherence with internal timelines and any external deadlines (e.g. approval expiration dates) through the use of various online research interface portals.
$68,000 - $78,514 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials in cardiovascular and chronic kidney diseases.
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The primary responsibility of the Clinical Research Coordinator is to manage all aspects of conducting clinical trials. As the primary resource for the protocols, the Clinical Research Coordinator will act as liaison between the investigators, primary care providers, the institutional review board (IRB), and the sponsor.
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Posted Job Title Abramson Cancer Center CRU Leukemia Program Manager Job Profile Title Manager Research Project B Job Description Summary The Abramson Cancer Center (ACC) of the University of Pennsylvania is a world leader in developing and conducting innovative clinical trials for the prevention, diagnosis, and treatment of cancer.
$61,046 - $95,524 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience working in a medical or clinical research setting (, psychology) EXPERIENCE: New graduates with some relevant course/project work or those without any prior research experience will be considered for the Clinical Research Coordinator I position outlined above.
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clinical research trials jobs Title: project manager clinical Company: Actalent
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