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(IRB), IACUC, PAM, the Institutional Biosafety Committee (IBC), and Conflict of Interest (COI). This position presents a unique and challenging opportunity to support and advance the university's world
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this position will report to Dr. Kathryn Taylor and to Dr. Randi Williams. To learn more, please see our website https://lunghealth.georgetown.edu/ . Requirements and Qualifications Bachelor's degree in pre-med
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Williams. To learn more, please see our website https://lunghealth.georgetown.edu/ . Requirements and Qualifications Bachelor's degree in pre-med, public health, psychology, or another social science is
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more about DOM CTU visit https://www.med.upenn.edu/pennctu/. Job Description Clinical Coordinator A: Participate in and coordinate clinical trials within the Penn Department of Medicine Clinical Trials
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Investigator’s (PI) guidance to meet the research objective of the project. Facilitates and implements study start-up activities including (but not limited to): trial feasibility assessment; study logistics; IRB
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Communication Center including, but not limited to, data collection, anonymizing data for analysis by faculty or student researchers, and distributing research materials to research subjects; maintain current IRB
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control and completion of clinical trials while assisting the Principal Investigator in regulatory oversight, preparation of IRB documents, data collection, quality control, recruitment and retention
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. Coordinates regulatory and research compliance activities, including preparation, submission, and maintenance of IRB protocols, amendments, continuing reviews, and communication with oversight offices. 7
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and quantitative imaging research, as well as support from dedicated staff for grant writing, IRB management, clinical research coordinat ors , image processing , and biostatistics. Faculty
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datasets, including routine quality-control checks and structured, well-documented file storage. Maintains regulatory and study documentation, assists with IRB submissions and amendments, and helps ensure