- Johns Hopkins University (Baltimore, MD)
- …will be part of a team that processes human subjects research protocols overseen by the Institutional Review Board ( IRB ). The IRB Coordinator ... human subject's research applications submitted to the IRB . + Determine level of review appropriate...extent permitted by the JHU equivalency formula. Classified Title: IRB Coordinator Role/Level/Range: ATO 37.5/03/OF Starting Salary… more
- 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 Colorado (Aurora, CO)
- …employment in an academic medical research environment + Experience submitting protocols to an institutional review board ( IRB ) + REDCap development and ... and using structured process improvement methods; and experience developing and submitting institutional review board protocols for community-based studies.… 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 Washington (Seattle, WA)
- …qualitative and quantitative research and data collection + Experience developing and submitting Institutional Review Board ( IRB ) proposal and ... Internal Medicine (GIM)** **has an outstanding opportunity for a** **Research Coordinator 2** **PostingTitle** **to join their team.** The University of Washington's… more
- University of Washington (Seattle, WA)
- …contribute writing IRB applications/modifications for complex research protocols. + Maintain Institutional Review Board ( IRB ) approvals and ... and identify opportunities for knowledge sharing. + Prepare and maintain study materials for the Institutional Review Board ( IRB ). + Draft and edit… more
- Stanford University (Stanford, CA)
- …procedures and reporting. + Demonstrated experience with regulatory requirements including Institutional Review Board requirements, HIPAA, and Good ... Research Program Coordinator in Precision Psychiatry **School of Medicine, Stanford,...or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, 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 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)
- …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
- Texas A&M University System (Kingsville, TX)
- …University-Kingsville regulations. This includes providing administrative and regulatory oversight for the Institutional Review Board ( IRB ), ... : + Coordinates the review and processing of research protocols for IRB ( human subjects), IACUC (animal research), and IBC (biohazards and recombinant DNA),… 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)
- …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...studies. Responsibilities include preparation of initial study documents for IRB submission in compliance with all local, state and… more
- Tufts Medicine (Boston, MA)
- …study sponsor and Institutional Review Board . 5. Assists with Institutional Review Board ( IRB ) requirements for each study including meeting ... Forms in accordance with best practice methods. 4. Complies with all institutional policies and government regulations pertaining to human subjects protections.… more