- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …meet the ongoing needs of the organization._ **Job Locations** _US-IL-Chicago_ **Title** _Senior Clinical Research Associate ( CRA )_ **ID** _2025-2205_ ... Sr CRA will be responsible for monitoring clinical studies at the site level ensuring...or related discipline. * 6+ years' experience as a Clinical Research Associate . * Extensive… more
- Parexel (Springfield, IL)
- The Senior Clinical Research Associate (Sr. CRA ) is responsible for the site management, site monitoring and close-out of assigned clinical ... needed + May undertake the responsibilities of an unblinded monitor where appropriate ** Clinical /Scientific and Site...+ Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably… more
- Parexel (Springfield, IL)
- **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA ) is responsible for the site management, site monitoring and close-out of ... Clinical Practices (GCP), and sponsor standards. The Sr. CRA is accountable for site management and...+ Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably… more
- IQVIA (Rosemont, IL)
- …help bring breakthrough treatments to patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate ( CRA ) to join our team ... **_IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year...will directly contribute to the integrity and quality of clinical research data. **Key Responsibilities** + Conduct… more
- Loyola University Chicago (Chicago, IL)
- …to interact with internal and external constituents. Certificates/Credentials/Licenses + CCRA (Certified Clinical Research Associate ) or equivalent (SoCRA or ... Clinical Research Coordinator II (IITs) Thank...Research Participants, Sponsors, and Regulatory agencies. + Coordinate multi- site studies from startup through close-out. Facilitate and manage… more
- Edwards Lifesciences (Chicago, IL)
- …in cardiology + Clinical research certification (ACRP or SOCRA, Clinical Coordinator/ CRA certification) + Prior clinical research experience ... within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with...a minimum of 5 years of work experience in clinical research monitoring, with a strong focus… more