Clinical Research Associate | Trials Monitoring & Travel
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Research/Development
Research Assistant/Associate, Clinical Research, Research Scientist -
Healthcare
Clinical Research
Job Description & How to Apply Below
ICON Strategic Solutions in Chicago is seeking a Clinical Research Associate (CRA I) to perform high-standard clinical trial monitoring within a sponsor-dedicated model. You will coordinate activities, maintain documentation, and ensure patient safety while collaborating with investigators and site staff.
The role requires 60% travel, strong knowledge of ICH-GCP, and excellent English communication. Employment is contingent on legal work authorization in the U.S.
For the Clinical Research Associate I | Trials Monitoring & Travel position at Regulatory Toolkit, we are reviewing applications now.
We are seeking a motivated Clinical Research Associate I | Trials Monitoring & Travel to join Regulatory Toolkit in Chicago, IL, United States.
Consider building your career as a Clinical Research Associate I | Trials Monitoring & Travel at Regulatory Toolkit.
The Clinical Research Associate I | Trials Monitoring & Travel position in the Bio & Pharmacology & Health field is open for applications.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
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