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The Research Nurse Coordinator, under the guidance and supervision of the Principal Investigator (PI) and the Medical Director, ensures the integrity and quality of clinical trials are maintained and conducted in accordance w/ federal, state, and local regulations, ICH/GCP guidelines, Institutional Review Board (IRB) approvals, and institutional policies and procedures.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Clinical Data Manager is responsible for data management oversight activities for research studies and works as an integral part of a cross-functional team through the lifecycle of the research study from design through final analysis and study closeout.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Prefer previous Clinical Research experience and previous experience with electronic data capture (EDC) systems. Enrolment of patients in several clinical trials as well as data entry, conduct and scheduling of follow-up visits, and regulatory support for research studies.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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POSITION SUMMARY:We are seeking a capable Jr. Clinical Research Associate (CRA) to be responsible for assisting the clinical team in planning, initiating, and monitoring Clinical trial sites as well as tracking enrollment and site engagement activities.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Incumbent will be supporting Senior Manager to achieve metrics related to activities in support of clinical trials, including design and maintenance of clinical databases using OpenClinica EDC, Veeva ETMF, decentralization tools, SAS; review of data collection forms; generation of data tables, listings and reports; establishment and documentation of data management processes.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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SAS, Programmer, statistics, CDISC, SDTM, ADaM, CRO, clinical research, pharmaceutical, biotechnology, clinical data, data management, EDC, Electronic Data Capture, Medidata, Rave, Oracle, Inform, datasets, TLF, tables, listings, figures, programming, benefits, medical, dental, vision, 401k, Remote.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Conduct Clinical Research Coordinator activities for assigned clinical research device studies including consenting participants, conducting study sessions, maintaining device accountability, and completing data entry into the Electronic Data Capture (EDC) system.
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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.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial. Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Manage Clinical Data Specialists to ensure all aspects of study data collection, management, and analysis meet the requirements to support regulatory submission of bioMrieux's molecular in vitro diagnostic products or other research activities.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Based out of New York, NY area, The Travel Clinical Research Coordinator primary responsibilities are to utilize Good Clinical Practices (GCP) in the process of screening, as well as enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
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Experience and/or knowledge of the healthcare data domain in at least one of: electronic medical records (EHR/EMR), clinical imaging, clinical workflows; Electronic Data captures (EDC), and/or clinical research/trials.
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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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We are looking to add a Per Diem nighttime Clinical Research Nurse to the team. It is a per diem schedule, open to 10 or 12 hour shifts, previous experience in clinical research isn't necessary but is preferred.
$100,000 - $125,000 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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2+ years of experience as a research assistant, data coordinator, laboratory personnel, or equivalent experience in a clinical research setting. Clinical Research Coordinator I.
ExpandApply NowActive JobUpdated 10 days ago
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