- Edwards Lifesciences (Sacramento, CA)
- …lives. Join us and be part of our inspiring journey. We are searching for a ** Clinical Research Monitor ** to join Edwards Field Monitoring team. As a ... Clinical Research Monitor , you ensure...Clinical Research Monitor , you ensure trial patients' safety... trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements. + Develop… more
- Edwards Lifesciences (San Francisco, CA)
- …us and be part of our inspiring journey. We are searching for a **Senior Clinical Research Monitor ** to join Edwards Transcatheter Pulmonic Field Monitoring ... team. As the Senior Clinical Research Monitor , you will...clinical trial/study safety in accordance with protocols, Good Clinical Practices (GCP), and regulatory requirements. +… more
- Stanford University (Stanford, CA)
- …of patient and research data in appropriate files per institutional and regulatory requirements. + Participate in monitor visits and regulatory audits. ... Clinical Research Coordinator Associate **School of...management and implementation of an assigned set of multiple research protocols assuring efficiency and regulatory compliance.… more
- Stanford University (Stanford, CA)
- …patients in person, interview patients, monitor follow-up, coordinate collection of clinical data and research samples as well as ensuring compliance and ... Clinical Research Coordinator Associate (1 Year...research data in appropriate files per institutional and regulatory requirements. + Participate in monitor visits… more
- Stanford University (Stanford, CA)
- …medical faculty in all aspects of clinical and translational research studies including regulatory compliance, study implementation, protocol development, ... Clinical Research Coordinator 2 **School of...with Microsoft Office and database applications. + Experience with research protocols and regulatory or governing bodies,… more
- Stanford University (Stanford, CA)
- …of patient and research data in appropriate files per institutional and regulatory requirements. + Participate in monitor visits and regulatory audits. ... Clinical Research Coordinator Associate (7 month.... **Duties include:** + Serve as primary contact with research participants, sponsors, and regulatory agencies.Coordinate studies… more
- Stanford University (Stanford, CA)
- …of patient and research data in appropriate files per institutional and regulatory requirements. + Participate in monitor visits and regulatory audits. ... Clinical Research Coordinator Associate **School of...diseases. **Duties include:** + Serve as primary contact with research participants, sponsors, and regulatory agencies.Coordinate studies… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator 2 **School of Medicine, Stanford, California, United States** Research Post Date Apr 25, 2025 Requisition # 106359 The Stanford ... Center for Clinical Research (SCCR)is a growing academic ...in Microsoft Office and database applications. + Experience with research protocols and regulatory or governing bodies,… more
- Stanford University (Stanford, CA)
- …of patient and research data in appropriate files per institutional and regulatory requirements. + Participate in monitor visits and regulatory audits. ... Neuromuscular Clinical Research Coordinator Associate **School of...Associate (CRCA) to coordinate the oversight and implementation of research protocols assuring efficiency and regulatory compliance.… more
- Stanford University (Stanford, CA)
- …of patient and research data in appropriate files per institutional and regulatory requirements. + Participate in monitor visits and regulatory audits. ... Clinical Research Coordinator Associate (1 Year...Surgery. **Duties include*:** + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate… more