- University of Utah (Salt Lake City, UT)
- Details **Open Date** 12/04/2025 **Requisition Number** PRN43738B **Job Title** PS Clinical Site Monitor **Working Title** Clinical Site Monitor **Career ... Day **Work Schedule Summary** **VP Area** President **Department** 01345 - HCI Clinical Resrch Compliance **Location** Campus **City** Salt Lake City, UT **Type of… more
- CSL Behring (King Of Prussia, PA)
- … development experience is expected including experience of study data review /evaluation in a pharmaceutical or clinical study environment. + * Demonstrated ... (ICF), Medical Monitoring Plans (MMP), Safety Review Committee (SRC)/Independent Data Monitoring Committee (IDMC) Charters, and Clinical Study Reports (CSR).… more
- Stanford University (Stanford, CA)
- …strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials. + Oversee data management for research ... and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. + Knowledge of… more
- University of Utah (Salt Lake City, UT)
- …and overall clinical objectives. Record adverse event and side effect data and confer with investigators regarding reporting of events to oversight agencies. ... Rate Range** $57,976 -$70,000 DOQ **Close Date** 01/23/2026 **Priority Review Date (Note - Posting may close at any...clinical objectives. Record adverse event and side effect data and confer with investigators regarding reporting of events… more
- Stanford University (Stanford, CA)
- …database applications + Demonstrated knowledge of regulatory requirements including Institutional Review Boards, HIPAA and Good Clinical Practices + Knowledge ... Clinical Research Coordinator Associate **School of Medicine, Stanford,...and anxiety. The CRCA would perform duties involved with data processing as well as the recruitment and assessment… more
- Rochester Regional Health (Rochester, NY)
- …of the MBS Clinical Reviewer to ensure that procedure and follow-up data are entered into the MBSAQIP Registry within the prescribed data entry ... training and the MBSAQIP Registry Operations Manual) to optimize data entry. + The MBS Clinical Reviewer...annually, one of which must be the annual comprehensive review meeting. + The MBS Clinical Reviewer… more
- University of Michigan (Brighton, MI)
- …complex nature of Oncology Clinical Trials, a team comprised of clinical research coordinators specializing in data management, regulatory, or clinic ... Study Operations (GCPs) 5. Study and Site Management 6. Data Management and Informatics 7. Leadership and Professionalism 8....directly related experience in clinical research and clinical trials is necessary. Please review SoCRA's… more
- Lilly (Boston, MA)
- …+ Ensure efficient database lock by overseeing monitoring plans and taking part in data review and reconciliation efforts. + Contribute to the development and ... subsidiary of Eli Lilly & Company within Lilly Research Labs, is a clinical -stage genetic medicines company established with a mission to solve the global health… more
- University of Pennsylvania (Philadelphia, PA)
- …health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C Job Profile Title Clinical Research Coordinator B ... will be to provide assistance and oversight with single-center and multi-center clinical research trials conducted within the Cardiovascular Medicine Division of the… more
- Cedars-Sinai (Los Angeles, CA)
- …protocol and research objectives. Responsible for completing case report forms, entering clinical research data , and assist with regulatory submissions to the ... **Primary Job Duties and Responsibilities:** + Completes Case Report Forms (CRFs). + Enters clinical research data into Electronic Data Systems (EDCs) that… more