- University of Colorado (Aurora, CO)
- …**University of Colorado Anschutz Medical Campus** **Department: Colorado Multiple Institutional Review Board - Office of Regulatory Compliance** **Job ... year basis. **Preferred Qualifications:** + Experience working with Institutional Review Boards or OHRP/FDA regulations regarding human subject research. +… more
- Vitalief (Livingston, NJ)
- …will support a leading hospital research center in Livingston, NJ, administering and overseeing Institutional Review Board ( IRB ) activities to ensure ... grow sustainably. The Role We are seeking an experienced IRB Coordinator Consultant to join the Vitalief...compliance with federal, state, and institutional regulations governing human subjects research. This… more
- University of Southern California (Los Angeles, CA)
- …research is performed as described in protocol. Serves as contact for subjects, study personnel, Institutional Review Board ( IRB ) and study sponsor. + ... study continuing review and study amendments to Institutional Review Board ( IRB...public health practice + Experience preparing and managing the human subjects/ Institutional Review Board… more
- Georgetown Univerisity (Washington, DC)
- …trial sponsors, Office of Human Subjects Protection, Office of Institutional Review Board and Office of Research Quality Assurance. The ... Institutional Review Board ( IRB ) and compliance offices. The Regulatory Coordinator ...+ Familiarity with regulatory and ethical requirements related to human subjects research (eg, IRB , FDA, ICH-GCP,… more
- Stanford University (Stanford, CA)
- …bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. IRB submissions. + 2-4 years ... Clinical Research Coordinator 2 **School of Medicine, Stanford, California, United...provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and… more
- University of Utah (Salt Lake City, UT)
- …notifications and submits amended protocols, summaries, and consents to the Institutional Review Board ( IRB ). 6. Submits study renewal applications ... of Food and Drug Administration ( FDA ) requirements, Office of Human Research Protection ( OHRP...its regulations may be referred to the Title IX Coordinator , to the Department of Education, Office … more
- University of Utah (Salt Lake City, UT)
- …notifications and submits amended protocols, summaries and consents to the Institutional Review Board ( IRB ). 6. Submits study start-up applications, ... Rate Range** $39,300 - $68,349 **Close Date** 01/21/2026 **Priority Review Date (Note - Posting may close at any...its regulations may be referred to the Title IX Coordinator , to the Department of Education, Office … more
- Mount Sinai Health System (New York, NY)
- …Assists in preparing grant applications and documents (for eg, Institutional Review Board , Grants and Contracts Office ). **Qualifications** + Bachelors ... **Job Description** The Clinical Research Coordinator assists in the daily activities of clinical...of research experience Non-Bargaining Unit, 857 - Rehabilitation and Human Performance - ISM, Icahn School of Medicine, Rehab… more
- University of Washington (Seattle, WA)
- …are multiple resources available within the University system (eg Grant and Contract Services, Institutional Review Board , Office of Industry Relations) ... Prepare interim reports for principal investigators, industry sponsors and Institutional Review Board to ensure...**D** **DITIONAL REQUIREMENTS** + Knowledge and prior experience with human subject's institutional review process… more
- Mount Sinai Health System (New York, NY)
- …information. Assists in preparing grant applications and documents (for eg, Institutional Review Board , Grants and Contracts Office ). We are seeking a ... **Job Description** The Clinical Research Coordinator assists in the daily activities of clinical...well as part of a team. + Familiarity with IRB processes, research ethics, and HIPAA compliance (preferred). **Responsibilities**… more
- University of Rochester (Rochester, NY)
- …interventional activities, to document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... internal equity considerations._ **Responsibilities:** Coordinates the activities associated with human subject research. RESPONSIBILITIES: - Coordinates the administrative details… more
- University of Maine System (Orono, ME)
- …including publications. + Experience with human subjects research and/or coordinating Institutional Review Board ( IRB ) compliance. + Experience ... Research and Evaluation Coordinator takes the lead in obtaining Institutional Review Board approval for studies involving human subjects that are… more
- Georgetown Univerisity (Washington, DC)
- …frequent communication with the Institutional Review Board ( IRB ) and compliance offices. The Regulatory Coordinator often serves as the primary ... research + FDA, ICH-GCP) Familiarity with regulatory and ethical requirements related to human subjects research (eg, IRB , + Strong attention to detail and… more
- Stanford University (Stanford, CA)
- …for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed. + Assemble ... Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United...IRB . Protect the rights, safety and well-being of human subjects involved in the clinical trials. **Duties include*:**… more
- Stanford University (Stanford, CA)
- … Subjects Panel. + Coordinate new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies. Complete annual reports ... Clinical Research Coordinator 2 - Surgical Planning **School of Medicine,...to Institutional Review Board , CSTA, FDA and other regulatory… more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... apply. **POSITION SUMMARY** **:** We seek a Clinical Research Coordinator to support the Wu Tsai Human ...applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are… more
- Mount Sinai Health System (New York, NY)
- …preparation and submission of grant applications and documents (eg, Institutional Review Board , Grants and Contracts Office ). **Qualifications** + ... **Job Description** The Clinical Research Coordinator is an entry human subjects...telephone calls. + Assists in the collection, analysis and review of experimental data for publication and presentation. +… more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... Cancer Clinical Research Coordinator 2 - CCT (Hybrid) **School of Medicine,...applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are… more
- University of Utah (Salt Lake City, UT)
- …Research Infrastructure, Systems and Management has an immediate opening for a Study Coordinator in the Population Sciences Trials Office and Adapt team at ... substituted for two years of related work experience) required. IRB CITI Course in the Protection of Human...its regulations may be referred to the Title IX Coordinator , to the Department of Education, Office … 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 2 **School of Medicine, Stanford, California, United...applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are… more