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Field
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disorders, under PI supervision. The person who takes this position may be responsible for multiple research studies simultaneously, coordinating with the PI, IRB, sponsoring agency, community and the study
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Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by
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Coordinator I - Department of Surgery Posting Number req26854 Department Surgery Department Website Link https://surgery.arizona.edu/ Location Tucson Campus Address Tucson, AZ USA Position Highlights The
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University of North Carolina at Chapel Hill | Chapel Hill, North Carolina | United States | 7 days ago
include: Project Management Preparing, submitting, and managing IRB applications and modifications Developing and implementing study timelines and activities Organizing study-related meetings (scheduling
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% Research administration responsibilities: -Participate in and prepare updates for regular study team meetings. -Collaborate with PI and other study staff on regulatory management: Preparing and managing IRB
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development Experience managing IRB protocols KEY RESPONSIBILITIES & ACCOUNTABILITIES The level and mixture of the duties may vary by position but typically include a combination of the following
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to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external
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accurate and complete records which may include, but are not limited to, signed informed consent, relevant IRB approvals, source documentation, Case Report Forms (CRF's), drug dispensing logs, and study
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here: https://itacademy.harvard.edu/ . Job Description Job Summary Research, design, document, implement, configure, and validate solutions to business needs. Solve highly complex technical problems. May
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Procedures (SOPs) & Work Practice Documents (WPDs) Oversee and ensure completeness in appropriate AE and SAE reporting requirements as well as Deviation reporting to sponsors and the IRB. Manages the workflow