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Review Board (IRB) on submissions, for PI approval. Tracks progress from submission to approval. Assist in developing supportive study documents such as informed consent forms, monitoring templates, study
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, screening, informed consent, and longitudinal follow-up, communicate study information to families, communicate all policies and procedures, and respond to all inquiries. Prepare study-related materials
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, completing required forms and reporting results, and regulatory submissions. Conducts data collection activities and may prepare analytical reports on study results. Follows established clinical study
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the neonatal intensive care unit, throughout the hospital, or in the outpatient setting. The CRA will be responsible for the screening, consenting, recruitment, and selection of patients. They will also prepare
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implementation, completing required forms and reporting results, and regulatory submissions. Conducts data collection activities and may prepare analytical reports on study results. Follows established clinical
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documents; monitoring the occurrence of adverse events and reporting to the PI, the study sponsor and the IRB, if any. Under the supervision of the PI, work with study staff to prepare for monitoring and
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to electrophysiology and pediatric cardiology and be included in the publication of manuscripts. Key Responsibilities: Collect, organize, enter data into electronic systems Files (TMF), and prepare reports. Troubleshoot
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Sciences at Boston Children's Hospital seek to hire a full-time Clinical Research Assistant responsible for executing all tasks associated with The HEALthy Brain and Child Development Study (HBCD). The study