- Johns Hopkins University (Baltimore, MD)
- …ensure proper reporting to study sponsors and regulatory bodies. + Prepare and submit Institutional Review Board ( IRB ) applications, amendments, and ... are conducted per protocol, GCP (Good Clinical Practice), and institutional guidelines. + Screen and recruit eligible study participants...+ Conduct the informed consent process in compliance with IRB and federal regulations. + Review… more
- Trinity Health (Ann Arbor, MI)
- … Nurses, Sub-Investigators, and Principal Investigator. + Acts as liaison between the Institutional Review Board ( IRB ), Investigator, clinical ... Michigan Cancer Research Consortium (MCRC). Works with all study sponsors ( federal and industry) to assure MCRC sites meet all standards associated with Human… more
- AdventHealth (Orlando, FL)
- …adherence to research protocols._ _Serves as liaison between Principal Investigators and the Institutional Review Board ( IRB ) and the Office of ... of research and administration._ _Reviews all elements of the current institutional IRB approved informed consent (IC) document, according to current FDA,… more
- Mayo Clinic (Jacksonville, FL)
- …sites and/or federal agencies regarding study status changes; Federal and Institutional Review Board ( IRB ) document preparation and submission; ... principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. Collaborates with research team to assess feasibility… more
- AdventHealth (Orlando, FL)
- …adherence to research protocols._ _Serves as liaison between Principal Investigators and the Institutional Review Board ( IRB ) and the Office of ... of research and administration._ _Reviews all elements of the current institutional IRB approved informed consent (IC) document, according to current FDA,… more
- Mayo Clinic (Rochester, MN)
- …sites and/or federal agencies regarding study status changes; Federal and Institutional Review Board ( IRB ) document preparation and submission; ... investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. + Collaborate with research team...of research protocols. + Ensure implementation of research protocols after IRB approval and provide… more
- Cedars-Sinai (Los Angeles, CA)
- …contact for long-term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of ... needed for study, and assists with study budget and patient research billing. This role will follow all federal , local, FDA, IRB , and HIPAA guidelines and… more
- University of Michigan (Ann Arbor, MI)
- …to/around Ann Arbor, Michigan. + Preparing and maintaining regulatory documentation, including Institutional Review Board ( IRB ) protocols, amendments, ... research projects, or administering behavioral interventions in research settings + Experience with IRB processes,...posted for a minimum of seven calendar days. The review and selection process may begin as early as… more
- Rush University Medical Center (Chicago, IL)
- …necessary. Uses discretion to resolve issues when unplanned events arise. * May assist with Institutional Review Board ( IRB ) assignments such as initial ... conducted in accordance with the study protocol, local, state, and federal guidelines related to epidemiologic/ behavioral/ translational research . Exemplifies… 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 ... team members in retrieval and provision of documentation required for IRB submission/renewals in accordance with guidelines; continuing review , modification,… more