(Senior) Clinical Research Associate (CRA)
IQVIA · Hong Kong +1 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
IQVIA seeks a Clinical Research Associate to perform site monitoring and management for clinical studies in Hong Kong and Guangzhou. The role ensures sites conduct studies according to protocol, regulations, and sponsor requirements while managing recruitment, documentation, and data quality.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline, or equivalent education and experience
- Minimum 2 years of on-site clinical trial monitoring experience
- Knowledge of Good Clinical Practice (GCP) and ICH guidelines
- Proficiency with Microsoft Word, Excel, PowerPoint, and mobile devices
- Strong written and verbal English communication skills
- Organizational, problem-solving, and financial management abilities
What you'll be doing
- Conduct site monitoring visits including initiation, ongoing monitoring, and close-out activities
- Develop and track subject recruitment plans with sites to meet enrollment targets
- Provide protocol training and maintain regular communication with study sites
- Evaluate site compliance with protocol and regulatory requirements; escalate quality issues
- Track study progress including regulatory approvals, enrollment, case report forms, and data queries
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.