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sponsor. Complete and audit case report forms (CRFs) for accuracy, with guidance as needed. Maintains documents as required by FDA guidelines. May maintain contact with IRB and prepare and submit IRB
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including submissions to IRB and internal ancillary committees. Prepares regulatory documents, including informed consent form, and other required regulatory documentation; Communicates with research
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Psychology Posting Number req27237 Department Psychology Department Website Link https://psychology.arizona.edu Location Tucson Campus Address Tucson, AZ USA Position Highlights The Department of Psychology
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Nurse. Responsibilities include assisting in the preparation of initial study documents for IRB submission in compliance with all local, state and federal regulations; advise the IRB of amendment
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Regulatory Coordinator II. The Clinical Research Regulatory Coordinator II will prepare, submit, and assist with multiple levels of research documentation, IRB submissions to UAB, WIRB, Advarra, and others
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graduate studies. Key Responsibilities and Accountabilities Data Management and Project Management Manage project administration activities, including Institutional Review Board (IRB) interactions
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Prepare and maintain IRB materials, ensuring compliance with approved procedures Oversee the ordering, inventory, and management of lab equipment and office supplies; collaborate with the finance and
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, cooperative education, or workforce development Experience managing IRB protocols KEY RESPONSIBILITIES & ACCOUNTABILITIES The level and mixture of the duties may vary by position but typically include a
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care. The link to our website is: https://www.uab.edu/onealcancercenter/ Please attach a current resume with this application. General Responsibilities To prepare, submit, and assist with multiple
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visits. Regulatory & Compliance Support Ensure all recruitment and pre-screening activities comply with IRB requirements, HIPAA regulations, and Good Clinical Practice (GCP) guidelines. Prepare and