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The Data Coordinator works within the clinical research program and supports 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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The Clinical Research Coordinator screens, enrolls and follows study participants, conducts data collection and entry, and performs noninvasive cardiovascular tests according to study protocols.
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Reporting directly to the Disease Team Project Manager, the Clinical Research Coordinator I is responsible for coordinating and managing clinical trials including providing all aspects of protocol management, including screening for patient eligibility, data collection and analysis, ensuring protocol compliance, adverse drug reaction reports, monitoring patient treatment and toxicities, laboratory and specimen submission, and maintenance of accurate and complete clinical research files.
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The OHSU Knight Cancer Institute Clinical Research Coordinator is responsible for implementation and overall management of oncology clinical trials. The Knight Prostate Cancer Research Program is seeking a Clinical Research Coordinator (TI Sr. Clinical Research Assistant) working on complex therapeutic interventional clinical research protocols and data management.
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Utilizes professional clinical skills, education and/or experience in project planning and implementation of data collection for complex clinical/health research trials.
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The Clinical Research Associate/Clinical Research Coordinator I (CRA/CRC I) works under general supervision to enroll eligible patients to clinical research protocols and manage all aspects of data collection and submission for multiple cancer studies.
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Work At Home Data Entry Research Panelist Jobs - Part Time, Full Time This work-from-home position is ideal for anyone with a diverse professional background, including administrative assistants, data entry clerks and typists, customer service reps or drivers.
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Under the direction of the research principal investigator and manager, the Clinical Research Coordinator I works collaboratively to support hematology, oncology, bone marrow transplant, and cellular therapy clinical trials for pediatric patients.
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The CRC encompasses all funded clinical trials within the Department of Medicine, including the disciplines of internal medicine, cardiology, GI, neurology, oncology and pulmonary and critical care medicine, as well as select studies with UCSF Fresno faculty in the departments of OB/GYN, emergency medicine, neurosurgery, pediatrics and psychiatry and Dermatology.
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The Senior Clinical Research Coordinator is responsible for the implementation of clinical studies at all levels, including but not limited to: study feasibility, IRB applications and related forms, data collection forms, patient screening and enrollment, data analysis, sponsor/IRB communications, verification of investigative procedures to accomplish research goals, and preparation of reports.
$66,331 - $95,451 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Contribute to assessing and implementing computational, algorithmic, and predictive analytics approaches to address assigned biomedical research questions in areas such as retrospective observational research, emulated clinical trials, clinical decision support and population health surveillance.
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The Clinical Research Coordinator (Senior or Intermediate) hired into this position will serve as a clinical research study coordinator for both single and multi-center, investigator-initiated and industry-sponsored studies and clinical trials (both FDregulated and non FDregulated.
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Reporting relationship to Asset Lead; Director, Group Lead; Associate Director, Asset Lead; Senior Manager, Asset Lead; Manager, Clinical Data Scientist, Clinical Data Sciences, CDS.
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Serve as Clinical Data Scientist and Trial Lead for one or more clinical trials assuming responsibility for all CDS activities including selection and application of data acquisition standards, Data Management Plan, selection of quality risk indicators, third party study data due diligence.
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The Clinical Research Coordinator (CRC) is responsible for overseeing the day-to-day operations of clinical trials designed to test the safety and effectiveness of new drugs.
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clinical research data collection trials manager jobs Company: Kaiser Permanente
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