CTA-Shanghai
IQVIA · Shanghai, China
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Trial Assistant position supporting Clinical Research Associates and regulatory teams in Shanghai. Responsible for maintaining trial documentation, managing clinical supplies, tracking case report forms, and ensuring compliance with study protocols and timelines.
What they're looking for
- High school diploma or equivalent
- Three years of administrative support experience
- Proficiency with Microsoft Word, Excel, and PowerPoint
- Strong written and verbal English communication skills
- Knowledge of Good Clinical Practice (GCP) and ICH guidelines
- Excellent organizational and time management abilities
- Ability to work effectively with clinical teams and external stakeholders
What you'll be doing
- Maintain and update Trial Master Files and clinical documentation systems tracking site compliance
- Prepare, handle, distribute, and archive clinical documents according to standard operating procedures
- Track and manage Case Report Forms, queries, and clinical data flow
- Assist with Clinical Trial Supplies handling and tracking information maintenance
- 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.