The Senior Clinical Research Coordinator will independently manage complex industry-sponsored clinical trials, overseeing study execution, regulatory compliance, and patient recruitment. They will also mentor junior staff, perform clinical procedures, and ensure high-quality data management throughout the study lifecycle. Candidates must possess an Associate’s or Bachelor’s degree in a scientific or healthcare discipline and at least 5 years of clinical research experience. Proficiency in GCP, FDA regulations, and the ability to perform clinical tasks like phlebotomy and ECGs are required.
Senior Clinical Research Coordinator – Gurnee, IL
Gurnee, Illinois, 60031
Full Time
Onsite
supports..pdf, .doc, .docx, or .txt file


