Clinical Trial Assistant
IQVIA · Overland Park, KS +2 more
Clinical OperationsFull-time$36k–$123kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
IQVIA seeks a Clinical Trial Assistant to support clinical research teams in maintaining trial documentation, managing case report forms, and coordinating clinical supplies across multiple sites. The role involves document management, regulatory compliance support, and potential site visit assistance.
What they're looking for
- Bachelor's degree
- 3 years of administrative support experience
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Strong written and verbal English communication skills
- Excellent organizational and time management abilities
- Knowledge of Good Clinical Practice (GCP) and ICH guidelines
- Familiarity with clinical trial protocol requirements
What you'll be doing
- Update and maintain clinical documents and Trial Master Files to track site compliance and performance
- Prepare, handle, distribute, and archive clinical documentation according to standard operating procedures
- Track and manage Case Report Forms, queries, and clinical data flow
- Assist with Clinical Trial Supplies handling and maintenance of tracking information
- Serve as central contact for clinical team communications and project correspondence
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.