- University Health (Seguin, 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
- 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 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
- 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
- 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
- Johns Hopkins University (Baltimore, MD)
- …Human Research Protections and Director of the Human Research Protections Program, Institutional Review Board ( IRB ) Chairs, OHSR Director of ... Compliance and leaders from the Research Environment Systems (RES), Office of Research ...Monitor the electronic process for submitting applications for IRB and ancillary reviews and offer solutions to address… more
- University of Maryland, Baltimore (Baltimore, MD)
- …collection and clarification, and general administrative duties. * Assist in the preparation of Institutional Review Board ( IRB ) and Health Insurance ... Portability and Accountability Act (HIPPA) protocol development and ensure compliance of research operations with protocols. May assist in developing and… more
- Stanford University (Stanford, CA)
- …procedures and reporting. + Demonstrated experience with regulatory requirements including Institutional Review Board requirements, HIPAA, and Good ... and coordinate coverage planning across research programs. Monitor in-office schedules and compliance with onsite...or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and… 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)
- … 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
- Stanford University (Stanford, CA)
- …applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, ... Human Subjects Panel. + Coordinate new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies. Complete annual… more
- Stanford University (Stanford, CA)
- …applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions ... Human Subjects Panel. + Coordinate new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies. Complete annual… more
- Stanford University (Stanford, CA)
- …applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, ... Cancer Clinical Research Manager - GI Oncology (Hybrid) **School of...+ Coordinate new protocol submissions, renewals, and revisions to Institutional Review Board for multiple… more
- University of Utah (Salt Lake City, UT)
- …of oncology, and oncology related research + Prior experience with Institutional Review Board ( IRB ) procedures + Strong written and oral ... four years of clinical research experience that includes regulatory compliance monitoring/auditing, IRB application submission, and experience in human… more
- Johns Hopkins University (Baltimore, MD)
- … monitor + Ensure on time reporting of specific safety-related events to the Institutional Review Board ( IRB ), DSMB, Federal Drug Administration ... study leader + Collaborate in study operational meetings to review safety and protocol compliance data, engage...Research Program Analyst Job Posting Title (Working Title): Research Program Analyst, Safety & Compliance (Neurology)… more
- Stanford University (Stanford, CA)
- …for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed. + Assemble ... documents, and complete study documents/case report forms. + Ensure compliance with research protocols, and review...and research data in appropriate files per institutional and regulatory requirements. + Participate in monitor… more
- Stanford University (Stanford, CA)
- …for completion and accuracy with source documents.Prepare regulatory submissions, and ensure institutional Review Board renewals are completed. + Assemble ... documents, and complete study documents/case report forms. + Ensure compliance with research protocols, and review...and research data in appropriate files per institutional and regulatory requirements. + Participate in monitor… more
- University of Miami (Miami, FL)
- …and participant compensation/reimbursement records. + Prepares and submits annual continuing reviews to the Institutional Review Board ( IRB ). + Notifies ... community agencies, and study sponsors. + Updates appropriate agencies (such as sponsors, IRB , etc.) regarding current status of research project. + Provides… more
- University of Miami (Miami, FL)
- …detail, proven experience in managing regulatory documentation and submissions to entities such as the Institutional Review Board ( IRB ) and the Food and ... compliance and supporting the integrity of our clinical research efforts. + Complete regulatory IRB submissions,...initial study requests, annual reviews and modifications to the Institutional Review Board ( IRB… more
