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The Department of Health and Clinical Outcomes at the Saint Louis University School of Medicine invite applications for a full-time, twelve-month faculty position specializing in Health Data Science and Outcomes Research.
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Responsible for coordinating and managing clinical trials including providing all aspects of protocol implementation, including screening for patient eligibility, data collection and analysis, ensuring protocol compliance, adverse drug reaction reports, monitoring patient treatment and toxicities, laboratory and specimen collection and submission, and maintenance of accurate and complete clinical research files.
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Performs study-related tasks and procedures, i.e. phlebotomy (does not have to be certified but can provide training), vital signs, urine collection, ECGs, BMI. Ensures that the source data is captured in real time and is accurately documented.
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Under the direction of a Research Coordinator or PI, participates in clinical research study activities; screens, obtains consent, and enrolls in study; performs a variety of duties involved in the collection, documentation, and reporting of clinical research data.
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Description :The Clinical Research Assistant is responsible for recruitment of participants into the Biospecimen Repository Core Facility (BRCF) for primarily cancer research.
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Support clinical research reporting for data review, quality control checks, and interim and final analysis. This Clinical Research Assistant II will be responsible for: Provide support for a new Diagnostic Center of Excellence.
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Assist in coordinating the details of the study and documentation concerning study protocols, patient scheduling, history work, data collection, data entry, data management, follow-up care, and compliance with federal, state, sponsor and institutional guidelines.
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The Clinical Research Assistant is responsible for coordination of investigator-initiated transplant studies for the Department of Surgery as directed by the Principal Investigator.
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The Research Assistant Clinical will support various research studies, including federal and nonfederal funded grants, clinical trials, and community-based projects, supervised by the Clinical Research Supervisor and Principal Investigator.
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The Senior Clinical Research Assistant will be responsible for recruitment, screening, scheduling, and data collection for research participants in addition to maintaining contact throughout their study participation.
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Assist Clinical Research Coordinators (CRC) with quality assurance (QA) and quality control (QC) on patient charts prior to entering into Electronic Data Capture (EDC) Filing and organizing regulatory and patient related documents.
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Position tasks:Recruiting patientsSee patients and handle all patient visits for the various studiesinformed consentHelping out in Medical recordsAssist other coordinators with various tasks, including data entryKeeping all protocol regulatory binders, lab certificates, reporting of SAE, administrating all protocol and consent form amendments, maintaining all form 1572's and corresponding CV'sMinimum qualifications:Must have a bachelors degree in a science (Biology, Psychology, etc.
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University of Maryland, Baltimore (UMB) is currently seeking a Clinical Research Technician Assistant to join the Department of Medicine, Division of Gastroenterology and Hepatology, Inflammatory Bowel Disease Section.
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Process Data Collection Forms i.e. log in, tracking, quality control as appropriate for the study. Basic ability to analyze data and accurately document and record results. Job Responsibilities:To provide general administrative support to the Clinical Operations Department and assistance.
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Process Data Collection Forms log in, tracking, quality control as appropriate for the study. Assist in quality control audits of clinical study documentation. Set up, organize and maintain clinical study documentation.
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data job Title: assistant clinical research in Phenix-city, Alabama
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