- UTMB Health (Galveston, TX)
- Clinical Study Monitor ( IRB ) - Provost...clinical research studies approved by UTMB Institutional Review Board ( IRB ). ... by the research community. + Establish 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
- Trinity Health (Ann Arbor, MI)
- …time **Shift:** Day Shift **Description:** As part of the Research Compliance Department, the Institutional Review Board ( IRB ) Administrator will join a ... policies and procedures. + Provides education and guidance to IRB members to assure that the board ...to meet or exceed regulatory requirements. Responsible for evaluating clinical studies and associated study … more
- Stanford University (Stanford, CA)
- …applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, ... Panel. + Coordinate new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies . Complete annual reports to … more
- Stanford University (Stanford, CA)
- …applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, ... Panel. + Coordinate new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies . Complete annual reports to … 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
- Morehouse School Of Medicine (Atlanta, GA)
- …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
- 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
- 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 ... Scientist function provides scientific expertise necessary to design and deliver clinical studies and programs. **Position Summary / Objective** + Will… more
- Catholic Health Initiatives (Lexington, KY)
- …/regulatory, documents, applications and forms, including but not limited to the applicable Institutional Review Board ( IRB ) application form(s), ... plans as needed. (35%) Quality Assurance / Performance Improvement + Implement and monitor clinical trials and research projects that meet CommonSpirit Health… more
- System One (Pittsburgh, PA)
- …for the Billing Compliance and Financial Support Unit within the office. Responsibilities: + Review clinical trial submissions from study team into central ... 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