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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. Join us as we continue to grow, the Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines.
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Clinical Research Coordinator page is loaded. Clinical Research Coordinator. Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials.
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Preferred: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) is preferred. Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification, along with a minimum of two years additional professional experience, will be considered in place of degree.
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Under direction of the Principal Investigator (PI) and Sponsored Project Administrator in the Pulmonary, Critical Care & Sleep Medicine Division, the Senior Research Coordinator will independently coordinate and be accountable for the overall administration of clinical research efforts for a variety of advanced research projects and clinical trials focusing primarily on pulmonary hypertension and related conditions.
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SUPERVISORY RESPONSIBILITY (if applicable): A Clinical Research Coordinator I does not have any supervisory responsibility. A Clinical Research Coordinator II may assist with the training and orientation of new staff members.
$33,000 - $47,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As members of the GW School of Medicine and Health Sciences faculty, MFA providers are teachers and mentors for medical students, residents, fellows, and researchers preserving the rich tradition of academics, research, and healing.
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The Medical Faculty Associates is looking for a clinical research nurse to join the Division of Infectious Diseases (ID) with responsibilities in clinical research operations.
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As the primary resource for protocols, the Clinical Research Coordinator acts as a liaison between the patient, investigator, Institutional Review Board and sponsor. The Clinical Research Coordinator II will coordinate and conduct the day-to-day operations of TRIAD ongoing studies in cardiovascular diseases.
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The research nurse coordinator may also be involved in other DONS research studies that may include research registries, Patient-Centered Outcomes Research Institute (PCORI) projects, and investigator-initiated studies of novel biomarkers, diagnostic imaging and technology to capture and predict performance of subjects with neurologic disorders.
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In accordance with the Mission and Guiding Behaviors; the Research Coordinator is responsible for implementing and managing oncology clinical research projects across Mount Carmel Health System (MCHS.
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The Clinical Research Coordinator II works independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
$64,500 - $100,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Clinical Research Coordinator I assists with all data and source documentation, adverse event reporting and maintenance of complete regulatory files, also as a part of the learning experience.
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Clinical Research Coordinator - Oncology (Plano Study Coordinator)Our Plano campus is looking for an experienced Clinical Research Coordinator who will play an important part in coordinating drug treatment research trials within the Hematology and Oncology teams, as well as observational studies.
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Department SSD Psychology - Staff and Temporary Employees - GalloAbout the Department This research position is for a full-time Research Study Coordinator to assist PI Gallo in coordinating a newly funded NIH research study.
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Collaborates closely with NCORP, Mount Carmel, and Zangmeister Cancer Center (ZCC) research staff; which may include Clinical Research Nurses, Clinical Research Associates, the Principal Investigator, the Director of Operations, Investigators and Regulatory Staff to ensure key federal/state/local regulatory objectives are met and that ethical obligations are kept.
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Title: clinical research coordinator Company: Alcanza Clinical Research
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