27 web-programmer-developer "https:" "https:" "https:" "https:" "https:" "Newcastle University" research jobs at Boston Children's Hospital
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equipment, lab area, and supplies in a neat professional manner. Sterilize and clean glassware and prepare media and other materials using appropriate procedures. Inventories supplies, alerts supervisor
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assistant will coordinate the daily operation activities of the ARIA initiative. They will be responsible for screening, consenting, recruiting, and selecting participants. They will prepare IRB documentation
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Research, MIT to support research projects on developing medical devices for treating diabetes. This is a highly interdisciplinary project at the intersection of device engineering, materials science, and
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, affordable health, vision and dental insurance, child care and student loan subsidies, generous levels of time off, 403(b) Retirement Savings plan, Pension, Tuition and certain License and Certification
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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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Number: 150800448 Position Summary/ Department Summary: The Benderson Heart Center Clinical Research Program Center for Cardiovascular Genetics is seeking a highly motivated Clinical Research Assistant
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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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, 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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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