- 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
- University of Utah (Salt Lake City, UT)
- …Date** 07/22/2025 **Requisition Number** PRN42612B **Job Title** Pediatric Project Manager II **Working Title** Data Coordinating Center Project Manager II ... Rate Range** 58300 to 76624 **Close Date** 10/22/2025 **Priority Review Date (Note - Posting may close at any...has an immediate opening for a Clinical Project Manager II . Come be part of the Utah DCC where… more
- University of Pennsylvania (Philadelphia, PA)
- …laboratories. Ensure complete documentation, chain-of-custody, and compliance with biosafety, IRB , and institutional requirements. + Coordinate the conduct ... and document informed consent with participants and families in accordance with IRB and institutional requirements. + Schedule and coordinate study visits… more
- University of Southern California (Los Angeles, CA)
- …Coordinator (Research Nurse)Apply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/Protocol- Coordinator ... Nurse and has a strong interest in clinical research. The role of the protocol coordinator is a diverse one. This person works independently, yet is able to relate… more
- Rush University Medical Center (Chicago, IL)
- …vary depending on the circumstances of each case. **Summary:** The Clinical Research Coordinator II (CRC II ) independently coordinates assigned aspects of ... (CCRP), * Certified Clinical Research Associate (CCRA), * Certified Clinical Research Coordinator (CCRC), OR * Certified IRB Professional (CIP) **Job… more
- Georgetown Univerisity (Washington, DC)
- …dedication to making a difference in the world. Requirements The Clinical Research Coordinator 2 (CRC2) is responsible for managing and coordinating 7 out of ... week on site for these trials as the only coordinator for migraine/headache trials at our center, working exclusively...is part of a robust team of 6 CTM/CRC II s (including the CRC2), 2 Associate Directors, the… more
- Georgetown Univerisity (Washington, DC)
- …making a difference in the world. Requirements Job Overview Serves as clinical research coordinator for phase I, II , and III oncology clinical trials conducted ... of clinical research team. + Act as a liaison with hospital staff, physicians, IRB , review committees, clinical research finance team, and auditors. + Other… more
- The County of Los Angeles (Los Angeles, CA)
- …evaluation and genetic research evaluation, as well as grant writing and interaction with the Institutional Review Board ( IRB ). + Provides education to ... in connecting vulnerable populations, including those released from correctional and institutional settings to supportive housing. THE MISSION: To advance the health… more
- University of Utah (Salt Lake City, UT)
- …required. Some work travel may be required. **Responsibilities** **Clinical Research Coordinator (Non-R.N.), II ** Coordinate day-to-day clinical trial activities ... Rate Range** 50000 to 65000 **Close Date** 01/23/2026 **Priority Review Date (Note - Posting may close at any...at one of the following job levels:** **Clinical Research Coordinator (Non-R.N.), II :** Requires a bachelor's (or… more
- Veterans Affairs, Veterans Health Administration (Battle Creek, MI)
- …as well as the Medical Center's Research and Development Committee, and the local Investigational Review Board ( IRB ) (Ann Arbor). Outcome or other types of ... the VHA Education Loan Repayment Services program office after review of the EDRP application. Former EDRP participants ineligible...VACO protocols will have been preapproved by a national IRB and can be implemented as soon as available.… more
- University of Utah (Salt Lake City, UT)
- …External Posting **Pay Rate Range** 60700 to 85000 **Close Date** 11/01/2025 **Priority Review Date (Note - Posting may close at any time)** **Job Summary** The ... predictive modeling, data mining, and data management and managing IRB and DUA . The position requires attention to...perform the essential functions of the Biostatistician I and II positions **Work Environment and Level of Frequency typically… more