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The Research Nurse I provides direct patient care for clinical trials subjects. As one of the primary RN resources for pediatric HematologyOncology and stem cell transplant protocols, the Research Nurse I acts as a liaison between the patient, investigator, Institutional Review Board(IRB) and sponsor in carrying out the RN responsibilities of the protocol.
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Christiana Care Health System is currently seeking a Research Nurse Coordinator with two years of Oncology Clinical experience for our Cancer Research Department at the Helen F. Graham Center & Research Institute in Newark, DE.
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At each of our 12 multidisciplinary disease site centers, patients have a fully dedicated team that include oncologists, surgeons, navigators, and social workers, as well as a clinical research nurse at each MDC to explore avenues for potential cutting-edge treatments in the latest clinical trials.
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Serves as a preceptor and mentor for new or less experienced research nurse coordinators, clinical research associates, and support staff. Follows study-specific protocol guidelines, communicates, and interacts with investigators, hospital staff, department manager, sponsoring agencies, and others to effectively perform clinical research activities.
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Meticulously creates and maintains patient research charts containing source documents supporting all reported data. The 240,000 square-foot Graham Cancer Center is a multidisciplinary cancer center , or MDC, which means an entire team of our highly skilled specialists work together to create and implement a treatment plan as unique for the patient.
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This role plays a pivotal role in coordinating and overseeing clinical operations of all assigned Clinical Research Nurse and Clinical Trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research studies.
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The research psychometrist will perform activities including administering and scoring neuropsychological tests, as well as research participant recruitment, screening, and consenting, providing concierge-level service for all participant-facing interactions during the course of clinical trials and research studies.
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Experience: 3 years of experience in area of research specialty required Req ID : 1983 Working Title : Clinical Research Specialist I - Cheng Lab, Heart Institute Department : Heart Institute Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : EXEMPT Primary Shift : Day Shift Duration : 8 hour Base Pay : $31.13 - $52.92.
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The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs. Key Responsibilities In collaboration with other members of the clinical research site team works to ensure the execution of assigned studies.
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JOB DESCRIPTION AND POSITION REQUIREMENTS:The Penn State College of Medicine, Department of Family & Community Medicine, in Hershey, PA, is seeking highly motivated candidates for a Clinical Research Coordinator to implement and manage a clinical research study that aims to examine a blood-based cancer screening test on patient acceptance and compliance with colorectal cancer screening.
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The Senior Director, Dana-Farber Cancer Institute (DFCI’s) Clinical Research Network (CRN) oversees clinical research administration functions occurring outside of Boston’s Longwood Medical Center Area – including clinical trials activities and teams across DFCI’s Collaborative, External, and Regional Sites.
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Experience working in a medical or clinical research setting (, psychology) EXPERIENCE: New graduates with some relevant course/project work or those without any prior research experience will be considered for the Clinical Research Coordinator I position outlined above.
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Requirements: Job Title: Clinical Research Coordinator Location: Pittsburgh, PA, Hybrid: Combination of On-Campus and Remote work Schedule: Mon - Fri 8am to 5pm Type: Direct Hire Responsibilities: Work closely with the Principal Investigators, study/clinical staff assisting in the operations of ongoing clinical trials.
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Experience: 2 to 3 years of experience as a Clinical Research Coordinator. 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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Experience applying the following regulations and guidelines: Good Clinical Practice Guidelines, Health Information and Accountability Act (HIPAA), The Protection of Human Research Subjects, CHR regulations for recruitment and consent of research subjects, Effective Cash Handling Procedures, Environmental Health and Safety Training, Fire Safety Training.
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clinical research patient experience jobs Title: research assistant Company: Medix
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