- University Health (Pleasanton, TX)
- …OHRP Coordinate, monitor , and educate staff on best practices in research compliance and study execution Support grant applications, budgeting, and program ... research experience to a role that supports innovation, compliance , and excellence in human subject research ....play a vital leadership role in the coordination and review of complex human subject research protocols.… more
- University Health (San Antonio, TX)
- …OHRP * Coordinate, monitor , and educate staff on best practices in research compliance and study execution * Support grant applications, budgeting, and ... research experience to a role that supports innovation, compliance , and excellence in human subject research ....play a vital leadership role in the coordination and review of complex human subject research protocols.… more
- Wayne State University (Detroit, MI)
- Research Compliance Monitor , IRB Wayne...For-Cause Audits as requested by the Institutional Review Board Committee or Human Research ... compliance . Submit monitoring reports to the Human Research Protection Program Administration and to the Institutional...and protocol violations and direct to committee Chair, individual Institutional Review Board , institutional… more
- University of Pennsylvania (Philadelphia, PA)
- …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... responsibilities as assigned CRC-A + Prepare and process all Institutional Review Board ( IRB...institutional or study related committees and personnel (eg, IRB , DSMC, DSMB/Medical Monitor ) according to applicable… more
- University of Miami (Miami, FL)
- …a proven experience in managing regulatory documentation and submissions to entities such as the Institutional Review Board ( IRB ) and the Food and Drug ... compliance and supporting the integrity of our clinical research efforts. + Assist PIs and study team with...initial study requests, annual reviews and modifications to the Institutional Review Board ( IRB… more
- Stanford University (Stanford, CA)
- …applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, ... and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. IRB submissions. + 2-4 years clinical research coordinator… more
- Henry Ford Health System (Southfield, MI)
- …informed consent processes, and human subjects protection principles. + Coordinate with the Institutional Review Board ( IRB ) to facilitate efficient ... role serves as the central point of coordination for research education, IRB and IACUC compliance..., Reporting, and Continuous Improvement + Monitor compliance with institutional research policies… more
- Stanford University (Stanford, CA)
- …with all applicable institutional , regulatory, and federal requirements. Monitor Institutional Review Board ( IRB ) submissions and implement ... needed. + Serve as liaison between investigators, sponsors, and institutional offices. Monitor and report serious adverse...or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and… more
- University of Pennsylvania (Philadelphia, PA)
- …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... submissions and renewals in accordance with FDA and IRB guidelines + Assure compliance with the...of a team, as well as independently; knowledge of IRB and human research protection regulations; prior… more
- University of Pennsylvania (Philadelphia, PA)
- … visits in clinic; maintaining regulatory files; and preparing submissions to the Penn Biomedical Institutional Review Board ( IRB ) and central IRBs when ... and required tracking logs. Assemble and submit documents to institutional committees for study activation (eg, IRB ,...of a team, as well as independently; knowledge of IRB and human research protection regulations. This… more
