- 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 (Carlsbad, CA)
- …prior monitoring experience. * Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice ... 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
- 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
- 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
- Ochsner Health (Covington, LA)
- …bachelor's degree. Preferred - 2 years of experience in area of assigned clinical specialty, managing clinical research and patient databases. ... all documentation and regulatory submissions as required by the sponsor of the trial, regulatory agencies, research ...Skills and Abilities (KSAs)** + Knowledge of medical and clinical research terminology and processes. + Ability… more
- IQVIA (Overland Park, KS)
- Job Overview: Join our dynamic team as a Clinical Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites to ... ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking...from you! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: Coordination of clinical research studies. Performance of regulatory tasks including IRB and sponsor /CRO regulatory correspondence. ... Data collection and entry into paper and electronic databases. Maintenance of clinical research supply inventory. Processing clinical trial billing… more
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