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Responsibilities include; patient screening and recruitment, coordination of care of the research patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board (IRB.
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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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Provide compassionate clinical care and participate in research and clinical trials. Clinical Trials Oncologist. It is home to the Bio Innovation District, founded to foster a hub of bioscience research and entrepreneurship centered on the City’s downtown university campuses and medical facilities.
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The Clinical Trials Management Associate will work closely with Technical Operations to ensure drug product quality and delivery, Translational Sciences to ensure timely site biomarker sample collection and shipments, and support the clinical operations team with TMF filing and other duties as assigned.
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Analyzes, facilitates and participates in the daily activities of multiple moderately complex clinical trials and performs all aspects of clinical data management, including patient data retrieval, referring MD office records, preparing clinical research charts, and participation in program audits.
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Human Subjects' Research - As applicable, oversee the submission of necessary documents required by the NYU Institutional Board (IRB), NYU Office of Clinical Trials and any other appropriate parties in order to obtain approval to conduct human subjects research (e.g., ensures the update and submission of necessary documents and/or forms to appropriate destination.
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Identify, engage, and manage the activities of clinical CROs and other clinical study providers (e.g., core labs, Electronic Data Capture (EDC) providers, and independent contractors) to execute clinical trials.
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Research and Development (PRD), you will play a key role in the deployment of Client digital and imaging measures in clinical studies, collection, management and analysis of sensor data, both in patients and healthy volunteers.
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This position will involve internal CAP/CLIA lab support, assay development responsibilities and clinical trials support. The candidate should have a strong interest in providing pathology support for biomarker development programs across oncology and hematology as well as an interest in clinical trials support/enablement.
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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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Responsibilities: Conducting all trial visits Completing all study-specific assessments (e.g. vital signs, EKG, blood collection) Processing all samples and shipping to Central Lab Maintaining study source Entering data into sponsor EDC and query resolution as the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate must be adept at protocol comprehension and be capable of working autonomously.
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It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository.
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Sentara Heart Hospital located on the campus of Sentara Norfolk General Hospital is hiring a Cardiovascular Research Nurse to support the Clinical Trials Office! Research RN manages and coordinates all aspects of conducting clinical trials within Sentara Health, both clinically and administratively.
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Job Description: The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials.
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Experience: 2 to 3 years of experience as a Clinical Research Coordinator. The Sr. CRC applies critical thinking and creative problem-solving skills across a wide variety of clinical studies, and contributes to the development of new processes, procedures, tools and training to enhance clinical research activities and is accountable for adhering to quality standards.
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clinical trials data collection jobs Title: clinical research monitor
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