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The Travel Clinical Research Coordinator will be mentored by their CRC Lead, Site Manager, Senior Manager, and other leaders within clinical operations. Based out of the San Antonio, TX area, The Travel Clinical Research Coordinator Based primary responsibilities are to utilize Good Clinical Practices (GCP) in the process of screening, as well as enrolling andclosely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
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THE Clinical Research Associate (CRA) Role The CRA is an important member of the Alira Health Clinical team. Clinical Research Associate page is loaded Clinical Research Associate Apply locations Boston-Remote time type Full time posted on Posted 2 Days Ago job requisition id JR000112 Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration.
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Understanding of basic anatomy and physiology, electrophysiology and arrhythmiasRegistered Nurse with previous clinical research experience as either a CRA or Study Coordinator. POSITION SUMMARY:The Clinical Research Associate II (CRA II) will be a key contributor to AtriCure’s clinical affairs department and primarily responsible for the site management of assigned clinical investigative CRA II will assist with the implementation and execution of study protocols and associated study documents for clinical trials, including clinical monitoring of AtriCure also includes the coordination of site activities from site start-up to site closure as needed.
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Performs literature reviews in preparation for investigator-initiated studies; assists PI with drafting protocols, abstracts, presentations and manuscripts as neededThe successful applicant for the position of Clinical Research Coordinator will be knowledgeable about technology related advancements in the Orthopaedic field.
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The Clinical Research Coordinator (CRC) is an integral and essential member of the ACC CRU Research Team. We are looking for an enthusiastic, professional and committed team member to work closely with our clinical research investigators, Research Team Leaders, our clinical research nurse(s), and regulatory coordinator.
$43,919 - $66,183 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Years experience: Minimum of two (2) years experience coordinating research protocols OR (2) years experience in cancer research OR certification as a Certified Clinical Trial Investigator (CCTI), Certified Clinical Research Coordinator (CCRC), or Certified Clinical Research Professional (CCRP) from the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SoCRA.
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GDIT's Military Health Team is seeking an Assistant Clinical Research Coordinator in support of the Naval Health Research Center (NHRC) Operational Infectious Disease (OID) Field Surveillance and Laboratory Research Services.
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About this opportunity This Clinical Research Associate- Contractor is responsible for monitoring and tracking patients in clinical studies at Align Technology and ensure that the studies are conducted according to protocol.
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The Clinical Trial Rater, a mental health professional, will be solely responsible for interviewing research participants and their informants/caregivers who are being evaluated to participate in a research study for various cognitive and behavior disorders.
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We research, develop, and commercialize innovative digital health products and solutions by bringing together the full capabilities of our team, including product strategy and management, clinical expertise, partnerships, UI/UX design, usability research, clinical research and validation, software development, AI / Gen AI, and regulatory submissions.
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Due to our continued growth, we are hiring for a Clinical Trial Rater at Wake Research, an M3 company. M3 Wake Research is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs.
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Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it.
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The CRC B (Regulatory Coordinator) will assist with preparing and processing regulatory documents through the IRB and other research review boards and have the ability to handle a variety of clinical trial related regulatory responsibilities in accordance with University of Pennsylvania, GCP, ICF, and FDA guidelines.
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The Clinical Research Coordinator is responsible for coordinating and overseeing clinical operations of all assigned clinical trials and participates in assessing, planning, implementing and compliant study conduct according to all relevant local, federal, and state regulatory and institutional Polices and Standard Operating Procedures.
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Preferences Working knowledge of pediatric hematology/oncology clinical trials Laboratory experience processing tissue samples Credentialing as a Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or other related certification.
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clinical research jobs Title: operations ophthalmology
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