- IQVIA (Carlsbad, CA)
- …in lieu of degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Parsippany, NJ)
- …in lieu of degree. Req * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Parsippany, NJ)
- …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
- ThermoFisher Scientific (Las Vegas, NV)
- …the successful completion and filing of case report forms and source documents for clinical research studies. Works with sponsor representatives at all ... safety and positive impact on patient's lives. As a Research Team Clinical Data Associate ,...accurate and timely completion of study CRFs to meet sponsor requirements and deadlines. Informs Research Team… more
- Stony Brook University (Stony Brook, NY)
- Clinical Research Associate II **Required Qualifications (as evidenced by an attached resume):** Bachelor's Degree (foreign equivalent or higher).Three (3) ... a private educational corporation. Employment is subject to the Research Foundation policies and procedures, sponsor guidelines...of posting.** **Job Number:** 2503665 **Official Job Title:** : Clinical Research Associate II **Job… more
- Rush University Medical Center (Chicago, IL)
- …disability, veteran status, and other legally protected characteristics. **Position** Associate Clinical Research Coordinator **Location** US:IL:Chicago ... works under the general direction of the Office of Research Affairs' Clinical Research Administration...and responds to questions from PI, Administrator, Office of Research Affairs, Sponsor and Compliance throughout the… more
- Alameda Health System (Oakland, CA)
- Clinical Research Associate + Oakland, CA + Highland General Hospital + HGH Opioid Use Disorder Grant + Services As Needed / Per Diem - Day + Allied Health + ... of the Manager of Grants & Special Projects, the Clinical Research Associate coordinates all...and screening requirements. Reports serious adverse events to study sponsor and FDA, when appropriate. Ensures compliance with all… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Sep 10, 2025 Requisition # 107255 ... The Stanford Stroke Center is seeking a Clinical Research Coordinator Associate to...databases, and regulatory files. + Participate in monitoring visits, sponsor meetings, and regulatory audits, serving as the study… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: The Clinical Research Associate I will be responsible for the coordination of clinical research studies within the Department of ... data collection and entry into paper and electronic databases. Maintenance of clinical research supply inventory, processing clinical trial billing… more
- Lilly (Indianapolis, IN)
- …at the highest level for efficiency and effectiveness. Reporting to the Director/ Associate Director Clinical Research Engagement Solutions, this ... and issues flagged directly or indirectly (eg through the Clinical Research Liaisons) + Ensure timely site...needed. + Assist sites with navigation or troubleshooting of sponsor systems (eg, IRT, EDC, eTMF, CTMS) and escalate… more
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