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expected to follow standard operating procedures (SOP) and associated environmental health and safety (EHS), human institutional review board (IRB) and institutional animal care use committee (IACUC
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, regulatory requirements, project timelines, and quality assurance procedures. Responsibilities include coordinating regulatory activities and IRB submissions; managing recruitment and engagement of CAP
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robotic technologies. Assist in IRB protocol development and ongoing human subject documentation. Conduct electromyographic ( EMG ) recordings and signal processing to analyze motor control and performance
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trial focused on muscle-driven robotic technologies. Assist in IRB protocol development and ongoing human subject documentation. Conduct electromyographic ( EMG ) recordings and signal processing to
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and industrial partners. Additionally, the role will involve the weekly organization and quality checking of survey data to ensure all documented IRB protocol procedures are followed and data is
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with other clinical or industrial partners. Additionally, the role will involve the weekly organization and quality checking of survey data to ensure all documented IRB protocol procedures are
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conferences. The ideal candidate will have experience in human subjects research, IRB documentation, fundamental biomechanics experiments, wearable sensing, and assistive robotics. Basic Qualifications Ph.D
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the post The Research Assistant will be responsible to provide research administrative/secretariat support such as Institutional Review Board (IRB) application/management, tracking of research Key
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. · Manage IRB submissions, reporting and management of studies. · Mentoring undergraduate and graduate students in their work on grant-funded projects. · Active dissemination of research in the
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, protected time and statistical and data support, prioritizing projects of greatest scientific and institutional value. Regulatory Compliance. Ensure all research adheres to IRB, institutional