Senior/Clinical Research Associate(Beijing/Shanghai/Guangzhou/Other Cities)
IQVIA · Shanghai, China +1 more
Clinical OperationsFull-timeCompany career page
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Role summary
Clinical research associate responsible for site monitoring, protocol compliance, and data management across clinical trial locations. Ensures sites conduct studies per protocol, regulations, and sponsor requirements while managing recruitment, documentation, and quality oversight.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline; equivalent education and experience accepted
- Minimum 1 year of on-site clinical trial monitoring experience
- Knowledge of GCP and ICH guidelines and regulatory requirements
- Proficiency in Microsoft Office (Word, Excel, PowerPoint) and standard computer platforms
- Strong written and verbal English communication skills
- Organizational and problem-solving abilities with effective time management
What you'll be doing
- Conduct site monitoring visits including initiation, ongoing monitoring, and close-out activities per protocol
- Develop and track subject recruitment plans with sites to meet enrollment targets
- Administer protocol training and maintain regular communication with study sites
- Evaluate site compliance with protocol and regulatory requirements; escalate quality issues
- Generate monitoring reports, follow-up letters, and maintain Trial Master File and Investigator Site File documentation
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.