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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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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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clinicians across LCCC consortium sites. Institutional Departments and Staff: Institutional Review Board (IRB), Office of Research Quality Assurance (ORQA), Clinical Research Operations Office, MedStar Health
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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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Number R260085 Posting Link https://www.ubjobs.buffalo.edu/postings/62900 Employer Research Foundation Position Type RF Professional Job Type Full-Time Appointment Term Salary Grade E.99 Posting Detail
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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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maintain regulatory documentation throughout the study lifecycle. Develop and submit IRB applications, amendments, continuing reviews, and reportable events through iRIS. Coordinate FDA submissions and
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Position Description We are hiring a research coordinator to facilitate the activities of grant-funded research (see https://sites.duke.edu/bablab/ ) and the Duke Interdisciplinary Behavioral
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blood and other biospecimen collections, administering surveys, performing data entry, and carrying out quality assurance activities with minimal supervisory oversight. Strict compliance with IRB rules