- UTMB Health (Galveston, TX)
- Clinical Study Monitor ( IRB ) - Provost...clinical research studies approved by UTMB Institutional Review Board ( IRB ). ... more
- Emory Healthcare/Emory University (Atlanta, GA)
- …+ Performs related approved responsibilities as required. JOB SPECIFIC DUTIES: 1. Study Coordination: Oversee the day-to-day operations of clinical research ... more
- Stanford University (Stanford, CA)
- …applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions ... more
- UTMB Health (Galveston, TX)
- … Research Monitor or Coordinator experience + Experience with a Clinical Trial Management System (CTMS), electronic IRB platform and EMR **LICENSES, ... more
- Touro University (Hawthorne, NY)
- … team. + Ensure compliance with the Good Clinical Practice guidelines in clinical research. + Monitor study patients for adverse events in collaboration ... more
- University of Miami (Coral Gables, FL)
- …to facilitate the smooth execution of clinical studies . + Monitor adherence to regulatory requirements, institutional policies, and Good Clinical ... more
- Bristol Myers Squibb (Princeton, NJ)
- …site and CRA training materials and present these at SIVs and Investigator meetings * Review clinical narratives * Monitor clinical data for specific ... more
- System One (Pittsburgh, PA)
- …the schedule of events for any projects. + Schedule of events off the protocol + Review clinical trial submissions from study team into central office for ... more
- Bristol Myers Squibb (Princeton, NJ)
- …materials and present these at SIVs and Investigator meetings. + Review clinical narratives. + Collaborate cross-functionally to monitor clinical data ... more
- University of Colorado (Aurora, CO)
- …and oversee the day to day operations of clinical trials and studies + Obtain study subject's medical history and current medication information, reviews ... more