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submission of study related documentation; prepares reports for organizations and agencies. Prepares or assists in preparing audit reports, IRB documents, and protocols. Recognizes, tracks and reports adverse
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this position will support is the “Pause to Protect” program (https://pausetoprotect.org/ ). This Department of Defense (DOD)-funded program engages a network of firearm businesses near ten military installations
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resolution of any issues that may arise throughout the study. Participate in preparing necessary documentation for Institutional Review Board (IRB) and NIH, together with the Principal Investigators
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, HIPAA, IRB and institutional and sponsor guidelines. Attends continuing education and compliance training as necessary. Conducts literature reviews to support grant proposal development. Prepares and
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federal, state or international requirements, while adhering to policies of The University of Kansas Medical Center. This position will be the assigned contact for study-start up activities including IRB
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Taylor and to Dr. Randi Williams. To learn more, please see our website https://lunghealth.georgetown.edu/ . Requirements and Qualifications Bachelor's or Master's degree in pre-med, psychology, public
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appropriate. Pre-initiation As appropriate & with guidance, reviews consent forms prior to submission to the IRB. With guidance, prepares other forms required for study initiation (pre-printed orders
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all aspects of clinical research including study planning and start-up, IRB management, identifying study patients, consenting and enrolling participants, lab procedures, as well as data collection
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to IRB and federal guidelines. Develops and implements policies and procedures; provides comprehensive direction to clinical research personnel; may participate in the hiring, training, and evaluation
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both the campus and medical center IRB. The Associate in Research will support administration of existing and future human subjects protocols. The Associate in Research will work under the direction