IQVIA LLC is seeking a Clinical Monitoring professional in Overland Park, KS, to ensure sites conduct studies per protocol and regulations. You will monitor, train, and manage site activities, data quality, and regulatory submissions, with strong communication to sponsor teams.
The role requires 1+ year of on-site monitoring, GCP/ICH knowledge, and proficiency in Word/Excel/PowerPoint. Collaboration with study teams and effective time/financial management are essential.
#J-18808-LjbffrClinical Research Associate: Site Monitoring & Coordination in overland park at Unknown Company
This position is listed as full time and onsite.