- Datavant (San Juan, PR)
- …management, partnerships, or business development. + Experience in **healthcare technology** , ** clinical research** , **EHRs** , **real-world data ** , or ... partner ecosystems that drive measurable business impact. + Deep understanding of CRO operations, data workflows, and the intersection of clinical trial data … more
- Loyola University Chicago (Chicago, IL)
- …of study specimens and processing. + Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop ... and processing. + Collect and manage patient and laboratory data for clinical research projects. Manage research...report forms. + Ensure compliance with research protocols, and review and audit case report forms for completion and… more
- HCA Healthcare (Nashville, TN)
- …**Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review ; monitors data for ... and research terminology** + **Computer skills including use of clinical trial database, electronic data capture, and...growth, we encourage you to apply for our Cardiology Clinical Research Nurse opening. We promptly review … more
- Stanford University (Stanford, CA)
- …clinical practice guidelines as well as collecting, recording and maintaining complete data files using good clinical practice in accordance with HIPAA ... and processing. + Collect and manage patient and laboratory data for clinical research projects. Manage research...include HIPAA and FDA regulations and Institutional policies. + Review Board requirements, and Good Clinical Practices.… more
- 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