- Johns Hopkins University (Baltimore, MD)
- …such forms. + Meets regularly with Principal Investigator, Research Nurse, and Research Program Manager to review regulatory accuracy and overall study ... Under the direct supervision of the GU Clinical Research Program Manager or the Principal...clinical studies which require a high level of knowledge, coordination , and data abstraction. Transmits and distributes protocol information.… more
- University of Michigan (Ann Arbor, MI)
- …2:1 Match on retirement savings **Responsibilities This position may provide study coordination for multiple clinical research studies, depending on the ... part of a team to develop and implement clinical research protocols preparing proposals for IRB approval...Minimum 2 years of directly related experience in clinical research and clinical trials is necessary. (Please review… more
- Mount Sinai Health System (New York, NY)
- …The Operations Manager will provide administrative, operational, and project coordination support to enable cutting-edge AI research and its translation ... and coordinating across collaborators and institutional departments. + ** Research Support:** Assist with IRB submissions, regulatory compliance, and… more
- Mount Sinai Health System (New York, NY)
- …This individual will report directly to the Medicine Clinical Trials Office (MCTO) Research Manager to assist with management of the electronic systems most ... Coordinator is responsible for ensuring regulatory compliance across US and international research sites. This role supports the coordination , submission, 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 ... work under the general direction of PACCM principal investigators and the Clinical Research Manager . Excellent computer skills are required including MS Word,… more
- University of Southern California (Los Angeles, CA)
- …overseeing compliance with protocols and standard operating procedures; and assisting with Institutional Review Board and regulatory compliance. The ... least 5 years of relevant experience in a clinical research coordinator or research manager ...and terminology. Knowledge and understanding of federal, state, and institutional research regulations including Good Clinical Practices… more
- University of Michigan (Ann Arbor, MI)
- …administrative study coordination and data entry support to faculty and research teams for the University of Michigan CS Mott Children's Hospital. Our program ... to a Clinical Research Coordinator Lead, Clinical Research Project Manager , Administrator, or Faculty Principal...Minimum 3 years of directly related experience in clinical research and clinical trials is necessary. (Please review… more
- Johns Hopkins University (Baltimore, MD)
- Reporting to the Senior Division Manager , Nurse Manager and or the Lead Research Nurse, we are seeking a **_Sr Research Nurse_** who will be responsible ... required regulatory documents. + May participate in drug data sheet development/ review /revision. + Monitors for IRB approval/request for further information… more
- University of Rochester (Rochester, NY)
- …the absence of the HSRC II. Serves as the liaison between cross-functional research team, study sponsors, and IRB to facilitate communication, resolves issues, ... GENERAL PURPOSE Under the direct supervision of the Clinical Trial Manager with direction from the Principal Investigators, coordinates all aspects of… more
- University of Utah (Salt Lake City, UT)
- …and fiscal management initiatives to enhance program efficiency and effectiveness in coordination with the Quality Assurance Manager 4. Forecasts and monitors ... Rate Range** 39300 to 72700 **Close Date** 12/01/2025 **Priority Review Date (Note - Posting may close at any...Knowledge of Good Clinical Practices, FDA , HIPAA and IRB regulations; an understanding of research procedures;… more