- Children's Hospital Los Angeles (Los Angeles, CA)
- …Day Shift **Purpose Statement/Position Summary:** Protection of human research participants - Institutional Review Board ( IRB ) review is ... research for submission to the IRB . The IRB Coordinator II , provides administrative... human research. + Experience conducting reviews of human research and working with an IRB … more
- Loyola University Chicago (Chicago, IL)
- …for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed. * Assemble ... Clinical Research Coordinator II Thank you for your...assisting in the preparation of initial study documents for IRB submission in compliance with all local, state and… more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... Clinical Research Coordinator II **School of Medicine, Stanford,...applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are… more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... Clinical Research Coordinator II **School of Medicine, Stanford,...governing bodies, which include HIPAA and FDA regulations, + Institutional Review Board requirements, and… more
- Vanderbilt University Medical Center (Nashville, TN)
- …REQUIRED** . KEY RESPONSIBILITIES + Proficiently prepares and processes new IRB research proposals, amendments, continuing review applications and adverse ... 20 **Job Summary:** **Device or Operating Room research experience REQUIRED IRB submission experience REQUIRED** This position will work with our Cerebrovascular… more
- Dialysis Clinic, Inc. (Albany, GA)
- …and post-study closure. They prepare documentation for submission for review by the Institutional Review Board ( IRB ), recruit and screen study ... including the collection, preparation, maintenance, and submission of numerous study documents: Institutional Review Board ( IRB ) applications, CV's,… more
- University of Utah (Salt Lake City, UT)
- …to the sponsor. * Liaison with central university research offices such as Institutional Review Board . * Prioritize workload with minimal supervision ... the clinical site. * Assist in the development of study protocols, managing human subject requirements, including IRB paperwork and procedures (new proposals,… more
- Seattle Children's (Seattle, WA)
- …contributing to groundbreaking discoveries in pulmonary health. As a Pulmonary Clinical Research Coordinator II , you'll be an integral part of this mission, ... collection instruments as required by study protocols. + **Document Review and Quality Assurance:** Assist in the thorough ...+ Knowledge of Good Clinical Practice (GCP) guidelines and human subject protection regulations (eg, IRB ). +… more
- University of Rochester (Rochester, NY)
- …trials involving greater risk to subjects). + Receives training and mentoring on conducting human subject research from HSRC II . + Provides support with study ... specimen processing and shipping. + Serves as back-up research coordinator in the absence of the HSRC II...Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee Program Required… more
- University of Pennsylvania (Philadelphia, PA)
- …research ethics and an interest in learning about IRB processes and human subject research regulations Clinical Research Coordinator B + Bachelor's degree ... A With increasing independence under supervision, the Clinical Research Coordinator A will coordinate Phase II and...detail-oriented, and able to multitask effectively + Familiarity with IRB processes and human subject research regulations… more