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Our research aims to improve quality of life, well-being, symptom and pain management, and reduce caregiver burden:For example, a Clinical Research Coordinator to support a large multi-site clinical trial study that focuses on the comparison of care delivery models to support older adults with complex healthcare needs.
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Support the data-management process for clinical research projects, including addressing data queries from data managers, project statistician, and sponsors. Follow direction of clinical research coordinator or others involved in the clinical research project work.
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This position may provide basic project management assistance to the leadership team (i.e. retrospective study set-up, case report form development, etc.) The Senior Clinical Research Coordinator-RN is an advanced position that involves a balance of study participant contact, research study initiation, coordination, and management of study data.
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This position requires close collaboration with the research team to ensure safe and compliant adherence to the research protocol and ancillary study activities. Join Avera as a Registered Nurse (RN) Senior Clinical Research Coordinator.
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2) Upload data into approved electronic records management systems and make copies of records available to NIH Principal Investigators (PIs) and protocol-specific staff. We offer a variety of full-time, project (SOW), seasonal, and surge support opportunities in science, engineering, technology, professional, and administrative support roles.
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O Responsible for creating appropriate protocol specific manufacturing and packaging work orders in concert with the clinical supply project manager. o Responsible for inventory management system set up activities (i.e. Material masters, manufacturing requests, etc) to support clinical packaging operations.
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Upload data into approved electronic records management systems and make copies of records available to NIH Principal Investigators (PIs) and protocol-specific staff. We are seeking an experienced individual to work as a Patient Care Coordinator at the National Institutes of Health in Bethesda, MD.
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Identifies, develops, communicates and tracks task completion dates , activities, logistics, and milestones in support of clinical supply project manager to ensure the timely availability of investigational drug supplies.
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Successful candidates will have experience working in semiconductor construction management industry, tool install preferred, proven ability to work autonomously and with teams of varying size and job function, have strong communication and organizational skills, possess strong project management capabilities, and thrive in an ever-changing project environment while leading teams to ensure on-time delivery of project scope.
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Expertise in project management related to tracking and managing assigned new protocol start-up packet; initiate, facilitate and monitor study start-up progress to ensure established benchmarks are met.
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Under the indirect supervision (minimal supervision) of the Principal Investigator (PI) and Project Manager (PM), the Clinical Research Coordinator B (CRC-B) will carry out research activities including recruitment, consenting participants, management of study materials, IRB submissions, device and supply management, biosample handling (collection, shipping and processing), and preliminary data analysis with manuscript writing.
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The Senior Clinical Research Coordinator serves as a key management and administrative role for the research project by supervising Clinical Research staff to ensure compliance with protocol, federal, and institutional requirements, and by frequently travelling to clinics to conduct trainings and site visits.
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Create Data Dictionary, as per protocol and in conjunction with principal investigator and statistician. Determine best method/s to identify potential participants for research protocol (advertisements, chart reviews, monitoring of clinic schedule, etc.
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Summary : PCR seeks a Clinical Research Coordinator who will be responsible for managing the day-to-day operations of assigned clinical trials, assisting in project planning, and ensuring that pre-established work scope, study protocol, and regulatory requirements are followed.
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May collect, process, ship, and maintain paperwork for blood and/or biological specimens according to procedures outlined in study protocol. Performs laboratory project as assigned by the Principal Investigator.
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protocol project management jobs Title: coordinator
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