- The George Washington University (Washington, DC)
- …to maintain engagement and conduct condom skills assessments. Uses REDCap system to monitor participant progress through the study , and ensure participants meet ... to the funder, attends and contributes ideas to team meetings, support for the clinical trial, assists in study instrument design. Supervises 3-4 hourly student… more
- 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
- The Mount Sinai Health System (New York, NY)
- …events to institutional offices and committees (ie Data safety monitoring, institutional review board , etc.) + Facilitates in/external monitoring and ... events (ie serial vitals) and the accurate capture of clinical data for the purposes of the study...analysis of clinical program activity data. + Monitor clinical trial portfolio and enrollments to… more
- Kelly Services (Van Nuys, CA)
- …Diagnostica, their own remote clinical trial management system, up to date + Monitor clinical studies . + Develop monitoring plans, identify issues, and ... keep clients and sites informed throughout the process. **Responsibilities** + Manage diagnostic clinical studies + Develop and manage the protocol, case report… 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
- GAP Solutions Inc (Baltimore, MD)
- …marginalized communities. + In depth knowledge of Institutional Review Board ( IRB ) regulations and Good Clinical Practice (GCP) guidelines - ... and update files of all applicable regulatory documentation for Institutional Review Board ( IRB...practices. 1 + Assist staff on all facets of clinical studies including subject enrollment, scheduling outpatient… 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, ... or governing bodies, which include HIPAA and FDA regulations, + Institutional Review Board requirements, and Good Clinical Practices. + Knowledge of… more
- University of Rochester (Rochester, NY)
- …in developing and overseeing the "on call" system for research staff to cover all active clinical studies + Monitor and track achievements of clinical ... & maintain the day-to-day operational duties of their assigned clinical trials and clinical research study...Obtain fully informed consent of all eligible trial & study patients in accordance to IRB , local… more
- Johns Hopkins University (Baltimore, MD)
- …recruiting and enrolling eligible patients into studies . + Prepare relevant documents for Institutional Review Board and as well for EPIC tracking. + ... diverse study teams and patient population. + Monitor the clinical course of patients enrolled...institutional and federal regulatory compliance, including preparing the IRB initial application, annual IRB continuing reviews,… more
- Hartford HealthCare (Bridgeport, CT)
- …goals outlined in the protocol and clinical trial agreement * Motivate others, monitor study performance and lead study meetings * Manage complex ... changes towards process improvement, leading efforts to initiate new studies , attending IRB meetings to expedite the...the compliance, financial, personnel and all aspects of the clinical study . *Job Responsibilities:* * Compiles and… more
