- Beckman Coulter Diagnostics (Miami, FL)
- …who possess various levels of clinical research experience.Ability to independently complete IRB submissions (initial review , change in research, continuing ... a part of the CCIA Clinical Affairs Team and report to the Clinical Affairs Manager responsible for planning and executing IVD clinical trials. If you thrive in a… more
- Dartmouth Health (Lebanon, NH)
- …Provides regulatory expertise, guidance and administrative support to the Dartmouth-Hitchcock (D-H) Institutional Review Board (s) ( IRB ). Responsible for ... concern to the HRPP Director or IRB Manager as appropriate. * Conducts non-committee review ...on applicable regulations, and subsequent submission in the electronic IRB protocol system. * Maintains D-H Collaborative Institutional… more
- Stanford University (Stanford, CA)
- …and relevant experience. **In addition, our preferred requirements include** : + Institutional Review Board professional certification desirable. **PHYSICAL ... IRB Manager **Dean of Research, Stanford,... IRB Manager **Dean of Research, Stanford, California, United States**...are seeking a candidate experienced with regulatory compliance and institutional review boards (IRBs) and that has… more
- Baptist Memorial (Memphis, TN)
- …clinical research facility and academic medical center Preferred: Proficiency with IRB - Manager software portal Education Minimum Requirement: High School ... Overview Summary The IRB Coordinator III works under minimal or no...supervision and acts as the lead staff for the IRB office. The IRB coordinator III does… more
- Stanford University (Stanford, CA)
- …by Human Subjects Panel. + Coordinate new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies. + Complete annual ... Lead Program Manager (2-Year Fixed-Term) **School of Medicine, Stanford, California, United...reports to Institutional Review Board , CSTA, FDA and… more
- AdventHealth (Orlando, FL)
- …Specialist I, provides regulatory support to the research team by handling all of the Institutional Review Board ( IRB ) and regulatory submissions and ... Regulatory Specialist I, functions as a liaison between the IRB of record for each study protocol and the...experience in healthcare, clinical research or scientific setting, an institutional review board office, or… 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 ... research related presentations. Works closely with the Principal Investigator, manager , and study team to identify problems and develop...AEs, SAEs, and UADEs reports to the Investigator and Institutional Review Board ( IRB… more
- Rush University Medical Center (Chicago, IL)
- …Pediatrics, and liaisons with the Principal Investigators (PIs), Industry Sponsors, the Rush Institutional Review Board ( IRB ), Corporate Compliance and ... of each case. **Summary:** The Clinical Research Regulatory Compliance Manager serves as the subject matter expert for a...staff; registers for trainings (EPIC, CITI, ONCORE, Rush Internal Review Board ( IRB ) portal, Rush… more
- Johns Hopkins University (Baltimore, MD)
- …through recruiting and enrolling eligible patients into studies. + Prepare relevant documents for Institutional Review Board and as well for EPIC tracking. + ... maintaining institutional and federal regulatory compliance, including preparing the IRB initial application, annual IRB continuing reviews, changes in… more
- Stanford University (Stanford, CA)
- …Human Subjects Panel. + Coordinate new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies. Complete annual ... Clinical Research Manager **School of Medicine, Stanford, California, United States**...reports to Institutional Review Board , CSTA, FDA and other regulatory… more
