- UTMB Health (Galveston, TX)
- Clinical Study Monitor ( IRB ) - Provost...clinical research studies approved by UTMB Institutional Review Board ( IRB ). ... the research community. + Establish a monitoring plan for IRB -approved studies including UTMB investigator-initiated projects. +...findings from monitoring visits. + Asses the conduct of clinical studies by monitoring compliance with the… more
- Stanford University (Stanford, CA)
- …applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions ... handling research administration activities associated with the conducting of clinical trials. Monitor staffing levels and identify...protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies .… 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 ... up-to-date and complete throughout the course of the research projects. 5. Clinical Monitoring: Monitor participants' progress throughout the trials, and… more
- UTMB Health (Galveston, TX)
- … Research Monitor or Coordinator experience + Experience with a Clinical Trial Management System (CTMS), electronic IRB platform and EMR **LICENSES, ... Coach is to provide mentorship, instruction and guidance to clinical research investigators, nurses, coordinators, and other study...study visits to provide support and feedback. 6. Review initial study documentation to ensure it… 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 ... institutional protocols. + Screen and enroll patients onto clinical trials in collaboration with clinical team,...mail, phone, fax, e-mail for COG, sponsored, local and multi- institutional studies . Act as liaison between NYMC… 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 ... by that unit. + Assist in preparing and submitting regulatory documents, including IRB applications, clinical trial protocols, and informed consent forms. +… more
- Northwell Health (New Hyde Park, NY)
- …human subjects research administrator to lead the establishment and oversight of a new Institutional Review Board ( IRB ) and its supporting administrative ... that meet the needs of the research community, establishing policies and procedures for IRB review and using data driven metrics to identify opportunities for… 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 ... system. + Maintain spreadsheets and systems designed to track study information. + Review IRB ...studies have entered OCT workflow per policy. + Monitor clinical research invoicing mailbox and route… more
- Philips (San Diego, CA)
- …**Your role:** + Play a critical role in the execution and monitoring of clinical studies from site start-up through close-out, ensuring compliance and data ... integrity. + Collaborate with Clinical Study Managers and cross-functional teams, including...informed consents, training materials, and device accountability logs. + Monitor clinical sites, track enrollment, verify source… 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 ... not move beyond this level.** This position will coordinate clinical research studies for the Depression and... study progress summaries for sponsors, independent site monitor for clinical trials, and independent monitoring… more