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Ensures antibody screen is obtained regularly per transplant center protocol (if applicable to organ). Collects and reviews data pertinent to recipients' health and organ function per protocol and as needed in follow-up.
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At Houston Methodist, the RN Clinical Communications Coordinator position a registered nurse, responsible for facilitating and coordinating patient care during all phases of transplantation. The Clinical Communication Coordinator position provides professional nursing care to a diverse patient population and interacts with all members of interprofessional transplant team to ensure coordination of care for the transplant patient.
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Minimum of 3 or more years of experience in clinical research as a Clinical Research Coordinator, with experience in patient consenting/retention; activation; regulatory compliance, data management, and ensuring Serious Adverse Events (SAEs) are completed and reported within reporting deadlines outlined in the protocol.
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GROWTH/INNOVATION ESSENTIAL FUNCTIONSAssists PI and/or research nurse in the planning and design of source documents for protocol. Under minimal supervision, this position is responsible for ensuring accurate data collection, documentation, organization and safety of research participants, gathering patient data for clinical research activities via methods specified in the study protocol and performs general administrative duties supporting the study.
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Maintains and monitors source documentation and appropriate forms as per protocol for quality and accuracy, including participant records; assists with the quality assurance process. At Houston Methodist, the Research Coordinator II position is responsible for coordinating the day-to-day activities of research protocols as well as assessing and determining qualification of patients for research studies.
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Obtains recipient blood type, tissue typing and cytotoxic antibodies according to transplant center protocol. RN Liver Transplant CoordinatorJob Summary We are looking for and Liver Transplant Coordinator - to coordinate all activities, at the highest quality of care for the transplant patient, family and living donor, at a developmentally appropriate level for patients served.
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Coordinates financial operations and assists with the planning of events and activities for the Office of Protocol and Special Events. This job is only available within the Office of Protocol and Special Events.
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Conduct face-to-face and/or telephone interviews with subjects, in accordance with interview protocol, data collection procedures and documentation standards. Contact potential subjects to introduce and explain study objectives and protocol and to arrange interviews, either in person or by telephone.
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The Clinical Studies Coordinator collaborates with the research team and principal investigator in managing research protocols, assuring protocol compliance, quality assurance and communicating with staff regarding protocol information.
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Collaboration with Clinical Research nursing staff, laboratory teams, hospital departments to ensure ongoing regulatory and protocol compliance. Qualifications: 2+ years of direct Clinical Research Coordinator experience, Strong patient interaction experience, Bachelor of Science.
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Helps direct the conduct of patients to ensure adherence to the research protocol and provides updates to Principal Investigator on study progress. Develops study binders for assigned protocols to outline guidelines for protocol compliance and to assure complete source documentation.
$45,000 - $65,000 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Helps with other ancillary tasks including but not limited to following up with patients that no-show or cancel surgical appointments, sending H&P orders and consents to outside hospitals, update surgical scheduler protocol handbook, constantly edit consents and documents as processes change, training sessions with our physicians, etc.
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Intermediate to advanced Excel experience, knowledge of accounting protocol in the general ledger, reconciliation of accounts, familiarity with accounts payable functions end‐to‐end. Intermediate to advanced Excel experience, knowledge of accounting protocol in the general ledger, reconciliation of accounts, familiarity with accounts payable functions end‐to‐end.
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The primary purpose of the Senior Coordinator, Clinical Studies is to provide day-to-day management and oversight of protocol compliance, patient care, and issues related to the coordination of clinical trials.
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Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials. DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator to join our team.
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protocol job Title: coordinator in Bellaire, TX
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