- HonorHealth (AZ)
- …Summary Coordinates all activities related to the Institutional Review Board and assures compliance with IRB guidelines and FDA regulations. In ... accordance with (45 CFR 46.101-409) the IRB Coordinator facilitates initial and continuing review ...This includes initial determinations regarding expedited, exempt, or full board review , as well as human subject… more
- RWJBarnabas Health (Long Branch, NJ)
- Assistant Director, Institutional Review Board - Long Branch, NJReq #:0000197806 Category:Laboratory and Medical Technologist Status:Full-Time Shift:Day ... Facility:Monmouth Medical Center Department: Institutional Review Board Pay Range:$102,960.00...accuracy, recommending the appropriate level of IRB review in accordance with federal and institutional … more
- Children's Hospital Los Angeles (Los Angeles, CA)
- …Subjects Protection Program in the areas of protocol reviews, liaison with the Institutional Review Board , and simple to moderately complex correspondence. ... **Minimum Qualifications/Work Experience:** 1+ years IRB experience. **Education/Licensure/Certification:** Bachelor's degree in a scientific or business discipline… more
- Brown University (Providence, RI)
- …of the BIRCH initiative (http://birch.brown.edu/) , Brown will soon be the main HRPP and Institutional Review Board ( IRB ) of record for Brown, Lifespan ... for the administration and implementation of the Human Research Protection Program (HRPP) and Institutional Review Board ( IRB ) policies and procedures… more
- Brown University (Providence, RI)
- …of the BIRCH initiative (http://birch.brown.edu/) , Brown will soon be the main HRPP and Institutional Review Board ( IRB ) of record for Brown, Lifespan ... implementation of the Human Research Protection Program (HRPP) and Institutional Review Board ( IRB...submissions in the electronic Huron system. The Associate HRPP Administrator also supports IRB Committee meetings by… more
- Sam Houston State University (Huntsville, TX)
- …compliance with Health Insurance Portability and Accountability Act ( HIPAA ), Institutional Review Board ( IRB ), Family Educational Rights and Privacy ... Act ( FERPA ), and institutional policies. Provides consultation and technical support to research...and publication. Supports data elements in grant proposals and IRB submissions; may be listed as key personnel on… more
- Rush University Medical Center (Chicago, IL)
- …on the circumstances of each case. **Summary:** Job **Summary:** The Research Administrator is responsible for leadership and oversight of the Grants Administration ... Team. The Research Administrator provides oversight of the entire departmental research portfolio...Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB Professional (CIP) preferred. * Advanced knowledge of the… more
- Cedars-Sinai (Los Angeles, CA)
- …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains research practices using Good ... responsibilities promoting activities and services associated with the Cedars-Sinai Board of Governors Innovation Center and associated Cedars-Sinai laboratories in… more
- University of Delaware (Newark, DE)
- Business Administrator I, Chemistry and Biochemistry Job no: 502146 College / VP Area:College of Arts & Sciences Work type: Staff Location: Newark, DE/Hybrid ... NIH Centers are complex entities that cut across departmental, college, and institutional boundaries. They have dozens of participants. At its inception, this center… more
- Cedars-Sinai (Los Angeles, CA)
- …to support research and grant activities. + Assist with regulatory submissions to the Institutional Review Board ( IRB ), including Adverse Events, Serious ... works directly with a Clinical Research Coordinator, Research Program Administrator , or Research Nurse to coordinate and/or implement the...patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB… more
- Cedars-Sinai (Los Angeles, CA)
- …patient contact for long term follow-up patients only. Assists with regulatory submissions to the Institutional Review Board ( IRB ) and works closely with ... works directly with a Clinical Research Coordinator, Research Program Administrator , or Research Nurse to coordinate and/or implement the...supervising research staff or directly with the Institutional Review Board to submit… more
- Cedars-Sinai (Los Angeles, CA)
- …for long term follow-up research participants only. *Assists with regulatory submissions to the Institutional Review Board ( IRB ) and works closely with ... works directly with a Clinical Research Coordinator, Research Program Administrator , or Research Nurse, or Principal Investigator to coordinate...supervising research staff or directly with the Institutional Review Board to submit… more
- Geisinger (Danville, PA)
- …Compliance, IRB Operations, Research Finance, and the Office of Institutional Advancement. + Demonstrates an understanding of federal regulations and guidelines ... Job Summary The Post-Award Administrator guides principal investigators, project directors, and project...annual OMB compliance supplement. + Maintains thorough knowledge of institutional policies as they apply to OSP processes and… more
- Cedars-Sinai (Los Angeles, CA)
- …for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... works directly with a Clinical Research Coordinator, Research Program Administrator , or Research Nurse to coordinate and/or implement the...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
- Carnegie Mellon University (Pittsburgh, PA)
- …supports research compliance requirements on supported awards includinghuman subjects ( IRB ) and animal (IACUC) protocols, clinical trials, export controls, andother ... compliance related requirements. + Program support may include supporting calls for projects by creating online submissionforms, assisting with coordinating web presence for specific programs, and point ofcontact for submissions, initial reviews and… more
- Cedars-Sinai (Los Angeles, CA)
- …for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... works directly with a Clinical Research Coordinator, Research Program Administrator , or Research Nurse to coordinate and/or implement the...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… 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 ... and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . *Maintains research practices using Good Clinical… more
- Cedars-Sinai (Los Angeles, CA)
- …term follow-up patients only. + Assists supervising staff with regulatory submissions to the Institutional Review Board ( IRB ) including submission of ... and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . Maintains research practices using Good Clinical… more
- Guidehouse (Bethesda, MD)
- …+ Track and review adverse event files and prepare reports in accordance with Institutional Review Board ( IRB ) processes and policies. + Prepare and ... and study applications, safety reports, annual reports and correspondence. + Coordinate with IRB administrator to collect, review and maintain all IRB … more
- Touro University (Valhalla, NY)
- …mentor-mentee relationships. + Ensure that students complete necessary training modules, such as Institutional Review Board ( IRB ) certifications, and ... credentialing/onboarding, and liaison with hospital affiliate administration and College IRB . + Oversee the development and implementation of research programs… more
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