Site Research Assistant - Kansas City, MO
IQVIA · Kansas City, MO
ResearchPart-timeCompany career page
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Role summary
This on-site position in Kansas City supports clinical research studies by performing data entry, maintaining regulatory documentation, and coordinating participant visits. The role requires managing study protocols, scheduling activities, and ensuring compliance with GCP standards and IRB requirements. An associate degree and 1+ years of clinical research experience are preferred.
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.