- HonorHealth (AZ)
- …Summary Coordinates all activities related to the Institutional Review Board and assures compliance with IRB guidelines and FDA regulations. In ... IRB Coordinator facilitates initial and continuing review of research protocols in compliance with...This includes initial determinations regarding expedited, exempt, or full board review , as well as human… more
- Trinity Health (Syracuse, NY)
- **Employment Type:** Full time **Shift:** Day Shift **Description:** ** Institutional Review Board Specialist - St. Joseph's and St. Peter's Health Systems** ... Summary** : Responsible for coordinating the operations of SJH/SPHP ( IRB ), the IRB Coordinator is...matters pertaining to protecting the rights and welfare of human research participants. + Ensures that submitted… more
- University of Rochester (Rochester, NY)
- …interventional activities, to document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... internal equity considerations._ **Responsibilities:** Coordinates the activities associated with human subject research . RESPONSIBILITIES: - Coordinates the… more
- University of Rochester (Rochester, NY)
- …the individual, and internal equity considerations._ **Responsibilities:** GENERAL SUMMARY The Human Subject Coordinator (HSRC) Trainee will assist with ... the Adolescent Brain and Cognitive Development (ABCD) Study, a federally funded research study in the Cognitive Neurophysiology Lab. General protocol and directions… more
- University of Colorado (Aurora, CO)
- …Office of Regulatory Compliance - Colorado Multiple Institutional Review Board ** **Job Title: IRB Panel Coordinator ** **Position #:00696471 - ... Review Boards or OHRP/FDA regulations regarding human subject research + Certified IRB...the Colorado Multiple Institutional Review Board (COMIRB) conducts reviews of submitted human … more
- University of Rochester (Rochester, NY)
- …+ Bachelor's degree or Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee Program + Or an equivalent ... of the individual, and internal equity considerations._ **Responsibilities:** GENERAL PURPOSE The Human Subject Research Specialist I (HSRS I) plays a vital… more
- Mount Sinai Health System (New York, NY)
- …in the preparation and submission of grant applications and documents (eg, Institutional Review Board , Grants and Contracts Office). **Qualifications** ... **Job Description** The Clinical Research Coordinator is an entry human subjects...telephone calls. + Assists in the collection, analysis and review of experimental data for publication and presentation. +… more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions and respond to ... Senior Research Coordinator in Precision Psychiatry and...applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are… 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 ... OBGYN has an exciting opportunity for a full-time Clinical Research Coordinator 3 to work in Miami,...initial study requests, annual reviews and modifications to the Institutional Review Board ( IRB… more
- University of Rochester (Rochester, NY)
- …met before enrollment. + Document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... forms and CRFs, are complete, accurate, and available for review . Communicates with Sponsor to clarify data queries to...Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee… more