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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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The Clinical Research Coordinator (CRC) will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical studies, ensures the timely collection and management of protocol-related samples, maintains regulatory binders, and ensures study compliance with state, federal, and IRB requirements.
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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.
$31.04 - $49.94 an hourFull-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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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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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 School of Medicine Clinical Trials Office (SOM CTO) is seeking a Clinical Research Senior Compliance Manager to manage the clinical research financial services provided by the SOM Clinical Trials Office.
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2 years of experience with each of the following: SAS and/or statistical programming; Databases & data management process; Statistical methods commonly used in pharmaceutical clinical trials; Pharmaceutics/Biotech/CRO clinical trials study analysis; Drug development & regulatory requirements; SAS programming/analysis skills; CDISC SDTM/ADaM requirements; and Clinical trial data management terminologies/processes.
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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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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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Work At Home Data Entry Research Panelist Jobs - Part Time, Full Time. To secure a legitimate work from home data entry position, expertise in that field isn't an absolute must. Roles include data entry clerk, customer service agent, nurse or medical assistant - just choose what suits your skills best and start earning.
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We are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida.
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clinical research data collection trials manager jobs Company: Brigham And Women's Hospital
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