- University of Utah (Salt Lake City, UT)
- …or knowledge of oncology, and oncology related research + Prior experience with Institutional Review Board ( IRB ) procedures + Strong written and oral ... assurance reviews, including monitor and audit visits on cancer related clinical trials to ensure compliance with study protocol, University, state and… more
- University of Colorado (Aurora, CO)
- ** Clinical Research Monitor (Entry Senior Level)**...is not limited to, the following: + Colorado Multiple Institutional Review Board (COMIRB) + ... Department of Medicine | Division of Hematology** **Job Title: Clinical Research Monitor (Entry - Senior Level)**...pharmaceutical firms or in-house staff for initial orientation to studies and for review of regulatory records.… more
- Alaka'ina Foundation Family of Companies (Camp Lejeune, NC)
- Institutional Review Board Administrative...the IRB Chairman and is accountable for IRB administrative matters to the Clinical Investigation ... Family of Companies (FOCs) is possibly looking for an Institutional Review Board Administrative Support...and serve as a resource, to co-workers in the IRB office. + Monitor the regulatory environment… more
- Alaka'ina Foundation Family of Companies (Silver Spring, MD)
- …training and education programs + Experience compiling and auditing clinical study packages for IRB review + Experience monitoring/auditing ... determinations. Verify the appropriate regulations are applied during the review of a study and validate that...EXPERIENCE: + Minimum three (3) years experience as a Clinical Trial Monitor + Knowledge and experience… 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
- Novant Health (Winston Salem, NC)
- …under the direction of their Novant Health leader in conjunction with study investigators. Clinical Research Coordinators facilitate and coordinate daily ... play a critical role in the conduct of the study . Our Clinical Research Coordinators are dedicated...clinical trial related activities. Collects, enters and summarizes clinical trial data. Monitor patients, their results,… 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
- University of Pennsylvania (Philadelphia, PA)
- …and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and assist in ... as needed and monitor results. Responsible for study coordination for investigator-initiated studies , multi-center research...AEs, SAEs, and UADEs reports to the Investigator and Institutional Review Board ( IRB… more
- Cedars-Sinai (Los Angeles, CA)
- …term follow-up patients only. + Assists supervising staff with regulatory submissions to the Institutional Review Board ( IRB ) including submission of ... the central hub of a full-circle approach to the study of inflammatory bowel disease (IBD). MIRIAD acquires, processes,...(FDA) and local Institutional Review Board . + Maintains research practices using Good Clinical… more
- University of Washington (Seattle, WA)
- …Generate initial drafts of human subjects' applications, consent forms and progress reports for institutional review board . * Serve as regulatory point of ... Study Coordinator 2 to work within our CVI Clinical Core. Under the general direction by the Director...maintain protocol adherence. * Assist in the design of studies and review proposals to determine appropriate… more
- University of Maryland, Baltimore (Baltimore, MD)
- …collection and clarification, and general administrative duties. * Assists in the preparation of Institutional Review Board ( IRB ) and Health Insurance ... the faculty member, for cancer patients enrolled in the studies . The Bone Marrow Senior Clinical Research...screening subjects for research studies according to IRB approved protocols. May communicate directly with study… more
- Stanford University (Stanford, CA)
- …with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed. + Assemble study kits for study ... Investigators conducting clinical research. Responsibilities include preparation of initial study documents for IRB submission in compliance with all local,… more
- University of Pennsylvania (Philadelphia, PA)
- …multiple clinical research projects investigating surgical outcomes in the US Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... multiple clinical research projects investigating surgical outcomes in the US Assist with Institutional Review Board ( IRB ) filings and inquiries, and… more
- Boston University (Boston, MA)
- …least 4 years experience working within human subjects research in positions such as IRB staff/analyst, study coordinator, or monitor /auditor is needed. + ... well as not-for-cause (Quality Assurance) reviews of human and clinical research studies at BMC and BU...within human subjects research in positions such as an IRB staff/analyst, study coordinator, or monitor… more
- University of Miami (Miami, FL)
- …and participant compensation/reimbursement records. + Prepares and submits annual continuing reviews to the Institutional Review Board ( IRB ). + Notifies ... assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies . This role assists in the day-to-day… more
- Stanford University (Stanford, CA)
- …applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, ... requests and questions. + Collaborate with principal investigators and study sponsors, monitor and report serious adverse...which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical… more
- University of Pennsylvania (Philadelphia, PA)
- …and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and assist in ... -related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.… more
- University of Pennsylvania (Philadelphia, PA)
- …and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and assist in ... to procedures as needed and monitor results. Responsible for study coordination for investigator-initiated studies , multi-center research studies ,… 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… more