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CTMS systems like CRIO, clinical conductor, Clinical Ink; EDC systems like MediData, Oracle, and Inform; ePRO, eConsent and IWRS/IXRS, etc. The Travel Clinical Research Coordinator will be mentored by their CRC Lead, Site Manager, Senior Manager, and other leaders within clinical operations.
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The CRA II will be responsible for the study start up process for AtriCure’s Clinical Investigational protocols, which includes and is not limited to the following: protocol review, Informed Consent Development, CRF design, EDC testing, preparation of site-specific logs/documentation and investigator study files.
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The Clinical Research Associate (CRA) for our global medical device client's team in Miami, FL is responsible for supporting clinical activities to generate clinical evidence that will support product registration and/or product market clearance/approval.
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Required: Must have experience as a Clinical Research Coordinator / 2 years+ of Chart review experience on EMR / 2+ years of EDC data entry. Data entry, Chart Review, Clinical Research Coordinator.
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Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed. Able to handle a variety of clinical research tasks. The Senior Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up to post database lock for assigned projects.
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Sr. Clinical Data Manager - Clinical Trial Services. Liaises with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables.
$80,000 - $120,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Fountain Group are a national staffing firm and are currently seeking a Clinical Research Associate for a prominent Medical Device client of ours. Clinical research certification (i.e., SOCRA, CCRA, CCRC.
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Function as a Clinical Data Manager (CDM) to coordinate the day-to-day support of CDM results from study start-up through to database lock to receipt of final study outputs for clinical studies outsourced to contract research organizations.
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Collaborate and consult with the MRDC's technical supporting team on the technical problem troubleshooting and system upgrade and maintenance activities of the MRDC in-house's Clinical Research Data Management System (CRDMS) and its components (e.g., Inform EDC, Central Designer, Central Coding.
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Coordinates study start-up activities; review and sign off of eCRF, eCRF completion guidelines, Data Validation Specifications, data management plan (DMP), data review guidelines (DRG); coordinates database live activities; tests/accepts clinical database for EDC studies.
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Directly (or indirectly via their staff) provide scientific and statistical / programming leadership for clinical trials including recommendation of appropriate research, sample size, appropriate statistical methodology, definition of patient and analyses populations, measurement of outcome variables, and hypothesis development.
$112,000 - $165,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As a Clinical Research Coordinator, you will abstract data from medical records, clinic, consultation, and referral notes to study forms and flow sheets; record data onto case report forms; and maintain source documentation for all case report entries.
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Review and query clinical trial data according to the Data Management Plan. Primary Data Management (DM) contact (Lead DM role) for assigned clinical project(s) / program(s), ensuring that there is back-up, continuity, responsiveness, and that tasks are performed in a timely manner.
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May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project. Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders.
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Solid understanding of clinical research methods, Clinical Data Interchange Standards Consortium (CDISC) principles, best data management practices and technologies related to clinical trials.
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