Sort by
Refine Your Search
-
Listed
-
Category
-
Country
-
Program
-
Field
-
of focus group recordings; review auto-generated transcriptions for accuracy Anonymize all transcripts according to IRB protocols (replace participant names/identifiers with participant codes) Maintain
-
about a job posting, please contact Human Resources at [email protected] . Department: RESH | Research Inst Review Board Department's Website: Summary of Job Duties: The Senior IRB Administrator
-
Position Information Position Information Working Title IRB Reliance Coordinator I, II or III Department Rsch Compliance, Integrity, Security-1315 Requisition Number S_260467 Posting Open Date 06/16
-
Position Information Position Information Working Title IRB Reliance Coordinator I, II or III Department Rsch Compliance, Integrity, Security-1315 Requisition Number S_260467 Posting Open Date 06/16
-
working at East Carolina University More Jobs from This Employer https://main.hercjobs.org/jobs/22391874/senior-irb-analyst Return to Search Results
-
(PI) guidance to meet the research objectives of the project. Assists with study start-up activities including IRB applications for initial review, modifications/amendments, continuing reviews, and
-
reports and follow-up letters, study manuals and other prepared study-related documents and templates, as requested by the QA Program and/or IRB. Authorized to request inspections due to data integrity
-
University of North Carolina at Chapel Hill | Chapel Hill, North Carolina | United States | 14 days ago
of the trial will be implemented at UNC. Collaborating with institutional partners (investigators, IRBs, CTRC, and IDS) to complete all tasks required for site activation (writing and submitting IRB applications
-
notes, and participant logs to help ensure safety. 7. Report and track adverse events (AEs). Reports serious AEs to PI, IRB and sponsor. 8. Review and manage clinical research study databases. 9. Educate
-
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 documents. May ensure proper