- 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 (Durham, NC)
- …in lieu of degree. * 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
- Rush University Medical Center (Chicago, IL)
- …the position. Offers may vary depending on the circumstances of each case. The Associate Clinical Research Coordinator will provide support and contribute to ... disability, veteran status, and other legally protected characteristics. **Position** Associate Clinical Research Coordinator **Location** US:IL:Chicago… more
- Rush University Medical Center (Chicago, IL)
- …disability, veteran status, and other legally protected characteristics. **Position** Associate Clinical Research Coordinator **Location** US:IL:Chicago ... on the circumstances of each case. **Job Summary:** The Clinical Research Coordinator I (CRC I) supports...events, and serious adverse events). 11. Work with PI(s), sponsor , compliance, clinical staff and/or manager to… more
- Hartford HealthCare (Hartford, CT)
- …to us. *Job Summary:* As a specialized research professional the Senior Clinical Research Associate (SrCRA) collaborates with the Principal Investigator ... these duties, the SrCRA works with the PI, department, sponsor , IRB and institution to support and provide guidance...all aspects of study activity as required of a Clinical Research Associate This is… 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 (1 Year Fixed-Term) **School of Medicine, Redwood City, California, United States** Research Post Date Apr 08, ... The Department of Orthopaedic Surgery is looking for a Clinical Research Coordinator Associate (CRCA)...uphold Stanford University's compliance with federal, state, local, and sponsor regulation. + Drive to establish themselves as a… 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
- 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